Fresh Recalls

FDA recalls — page 2

2,784 recent recalls from the U.S. Food & Drug Administration in our current data (last 90 days). Showing 301–600, newest first.

FDA Class II · Medical device · September 30, 2026

Evolution upgrade 1 recall — Philips North America Llc

A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the…

Company / brand: Philips North America recalls

Official ID Z-3235-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

Achieva XR recall — Philips North America Llc

A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the…

Company / brand: Philips North America recalls

Official ID Z-3234-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

Achieva 3 recall — Philips North America Llc

A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the…

Company / brand: Philips North America recalls

Official ID Z-3233-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

Achieva 1 recall — Philips North America Llc

A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the…

Company / brand: Philips North America recalls

Official ID Z-3232-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

VITEK 2 AST-N461 TEST KIT recall — Biomerieux Inc

The issue is related to card pouch damage associated with a portion of the lot which was produced on a specific card pouching device, in a specific timeframe, causing a potential r…

Company / brand: Biomerieux recalls

Official ID Z-3231-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

Medline convenience kits containing Healthmark Instrument Channel Brushes recall — Medline Industries, LP

Kits contain Healthmark Instrument Channel Brushes, which were recalled by the manufacturer due to the potential for a sharp edge/burr on the end of the brush. Potential hazards as…

Company / brand: Medline Industries recalls

Official ID Z-3230-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

Medline convenience kits containing Healthmark Instrument Channel Brushes recall — Medline Industries, LP

Kits contain Healthmark Instrument Channel Brushes, which were recalled by the manufacturer due to the potential for a sharp edge/burr on the end of the brush. Potential hazards as…

Company / brand: Medline Industries recalls

Official ID Z-3229-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

SeaSpine Mariner Deformity Product Name recall — SEASPINE ORTHOPEDICS CORPORATION

The proximal thread depth of the spinal device is out of design specification.

Company / brand: SEASPINE ORTHOPEDICS recalls

Official ID Z-3226-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

CombiSet Hemodialysis Blood Tubing Set with Attached Priming Set and Transducer Protectors recall — Fresenius Medical Care Renal Therapies Group, LLC

Communication to recommend reviewing the IFU and ensuring that all treatment preparation and handling steps are performed as instructed.

Company / brand: Fresenius Medical Care Renal Therapies Group recalls

Official ID Z-3225-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

PowerLED 300 Concealed Lighting System (PWD30+SF W K3 SPRING ARM A2 FC3 50-100nm) Model Nu recall — Maquet SAS

The potential for the device to detach at the junction between the spring arm and suspension arm and fall causing potential injury.

Company / brand: Maquet SAS recalls

Official ID Z-3224-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

REF recall — Ventec Life Systems, Inc.

Labeling; Oxygen Cylinders do not contain required medical gas labeling

Company / brand: Ventec Life Systems recalls

Official ID Z-3223-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

REF recall — Ventec Life Systems, Inc.

Labeling; Oxygen Cylinders do not contain required medical gas labeling

Company / brand: Ventec Life Systems recalls

Official ID Z-3222-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve recall — Ventec Life Systems, Inc.

Labeling; Oxygen Cylinders do not contain required medical gas labeling

Company / brand: Ventec Life Systems recalls

Official ID Z-3221-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

Midmark IQvitals Zone recall — Midmark Corporation

A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.

Company / brand: Midmark recalls

Official ID Z-3220-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

Midmark IQvitals Zone recall — Midmark Corporation

A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.

Company / brand: Midmark recalls

Official ID Z-3219-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

Midmark IQvitals Zone recall — Midmark Corporation

A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.

Company / brand: Midmark recalls

Official ID Z-3218-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

Midmark IQvitals Zone recall — Midmark Corporation

A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.

Company / brand: Midmark recalls

Official ID Z-3217-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

Olympus EZDilate Endoscopic Balloon Dilator Wired-guided 11 recall — Olympus Corporation of the Americas

Potential for the inflation chart label affixed to the shaft of the device to be incorrect and indicate a balloon diameter of 18, 19, or 20 mm,

Company / brand: Olympus of the Americas recalls

Official ID Z-3216-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

Brand Name recall — Heidelberg Engineering GmbH

Wheels may come loose when module is being pushed or pulled during movement or transportation, affecting stability of the stand. The stand may tip over as a result. Falling stand m…

Company / brand: Heidelberg Engineering recalls

Official ID Z-3215-2026 · Official record ↗

FDA Class I · Medical device · September 30, 2026

Imager II Angiographic Catheters M001314001 IMAGER II/5/ST/65/038 BX5 recall — Boston Scientific Corporation

Tip may fracture or detach, leading to device fragments remaining within the patient or migrating through the vasculature. Patient impact may include prolonged procedure or life-th…

Company / brand: Boston Scientific recalls

Official ID Z-3214-2026 · Official record ↗

FDA Class I · Medical device · September 30, 2026

Halyard IV START KIT NON-STERILE recall — AVID Medical, Inc.

Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may be contaminated with Aspergillus penicillioides.

Company / brand: AVID Medical recalls

Official ID Z-3194-2026 · Official record ↗

FDA Class I · Medical device · September 30, 2026

INCA (Infant Nasal Cannulae Assy) Neonatal Nasal CPAP recall — CooperSurgical, Inc.

Potential to exhibit a loose connection between the flexible tubing and the nasal cannula, during assembly or while in use, which may result in loss of CPAP pressure, possibly redu…

Company / brand: CooperSurgical recalls

Official ID Z-3140-2026 · Official record ↗

FDA Class I · Medical device · September 30, 2026

INCA (Infant Nasal Cannulae Assy) Infant Nasal CPAP recall — CooperSurgical, Inc.

Potential to exhibit a loose connection between the flexible tubing and the nasal cannula, during assembly or while in use, which may result in loss of CPAP pressure, possibly redu…

Company / brand: CooperSurgical recalls

Official ID Z-3139-2026 · Official record ↗

FDA Class I · Food · September 30, 2026

Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and black letteri recall — GIAS FOOD INC.

Contamination with Listeria monocytogenes

Company / brand: GIAS FOOD recalls

Official ID H-1396-2026 · Official record ↗

FDA Class I · Food · September 30, 2026

Fromagerie Coop de Mean Cabricharme and Belgium Cabricharme Shelf life recall — WFM Purchasing, LP

Undeclared Egg Allergen

Company / brand: WFM Purchasing recalls

Official ID H-1395-2026 · Official record ↗

FDA Class II · Food · September 30, 2026

So Delicious Dairy Free Salted Caramel Cluster Cashewmilk recall — WWF Operating Company

Product may contain foreign material: small stones and other hard objects.

Company / brand: WWF Operating Company recalls

Official ID H-1394-2026 · Official record ↗

FDA Class III · Food · September 30, 2026

American Ginsengs recall — Kwok Shing, Inc.

Potential contamination with pesticides.

Company / brand: Kwok Shing recalls

Official ID H-1393-2026 · Official record ↗

FDA Class II · Food · September 30, 2026

Powdered Sugar recall — United Sugar Producers and Refiners

Potential Wheat Kernel contamination.

Company / brand: United Sugar Producers and Refiners recalls

Official ID H-1392-2026 · Official record ↗

FDA Class II · Food · September 30, 2026

Light Brown Sugar recall — United Sugar Producers and Refiners

Potential Wheat Kernel contamination.

Company / brand: United Sugar Producers and Refiners recalls

Official ID H-1391-2026 · Official record ↗

FDA Class I · Food · September 30, 2026

Evergreen Fresh Sprouts LLC recall — Evergreen Fresh Sprouts LLC

Salmonella

Company / brand: Evergreen Fresh Sprouts recalls

Official ID H-1390-2026 · Official record ↗

FDA Class II · Food · September 30, 2026

Pecorino Toscano D recall — Elegant Foods, LLC

Potential Listeria contamination from dripping condensation in cooler.

Company / brand: Elegant Foods recalls

Official ID H-1389-2026 · Official record ↗

FDA Class II · Drug · September 30, 2026

Clear Eyes Redness Relief recall — Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company

Lack of Assurance of Sterility

Company / brand: Insight Pharmaceuticals recalls

Official ID D-0871-2026 · Official record ↗

FDA Class II · Drug · September 30, 2026

Clear Eyes Redness Relief recall — Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company

Lack of Assurance of Sterility

Company / brand: Insight Pharmaceuticals recalls

Official ID D-0870-2026 · Official record ↗

FDA Class II · Drug · September 30, 2026

Exenatide Injection recall — Amneal Pharmaceuticals of New York, LLC

Defective Delivery System: Possibility of no medication in the prefilled pen.

Company / brand: Amneal Pharmaceuticals of New York recalls

Official ID D-0868-2026 · Official record ↗

FDA Class III · Drug · September 30, 2026

Olanzapine Tablets recall — Macleods Pharmaceuticals Limited

Failed Impurities/Degradation Specifications:Organic and unspecified impurities above specification.

Company / brand: Macleods Pharmaceuticals recalls

Official ID D-0867-2026 · Official record ↗

FDA Class II · Drug · September 30, 2026

AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0 recall — Sterling Pharmaceutical Services LLC

Lack of Assurance of Sterility

Company / brand: Sterling Pharmaceutical Services recalls

Official ID D-0863-2026 · Official record ↗

FDA Class II · Drug · September 30, 2026

Lubricant Eye Drops-Cameron Pharmaceuticals recall — Sterling Pharmaceutical Services LLC

Lack of Assurance of Sterility

Company / brand: Sterling Pharmaceutical Services recalls

Official ID D-0862-2026 · Official record ↗

FDA Class II · Drug · September 30, 2026

Major LubriFresh P recall — Sterling Pharmaceutical Services LLC

Lack of Assurance of Sterility

Company / brand: Sterling Pharmaceutical Services recalls

Official ID D-0861-2026 · Official record ↗

FDA Class II · Drug · September 30, 2026

TRP The Relief Products* Gentle Eyes Lubricant Eye Drops recall — Sterling Pharmaceutical Services LLC

Lack of Assurance of Sterility

Company / brand: Sterling Pharmaceutical Services recalls

Official ID D-0860-2026 · Official record ↗

FDA Class II · Drug · September 30, 2026

Reliable-1 Laboratories Lubricating Tears recall — Sterling Pharmaceutical Services LLC

Lack of Assurance of Sterility

Company / brand: Sterling Pharmaceutical Services recalls

Official ID D-0859-2026 · Official record ↗

FDA Class II · Drug · September 30, 2026

Walgreens Lubricant Eye Drops recall — Sterling Pharmaceutical Services LLC

Lack of Assurance of Sterility

Company / brand: Sterling Pharmaceutical Services recalls

Official ID D-0858-2026 · Official record ↗

FDA Class II · Drug · September 30, 2026

Walgreens Lubricant Eye Drops recall — Sterling Pharmaceutical Services LLC

Lack of Assurance of Sterility

Company / brand: Sterling Pharmaceutical Services recalls

Official ID D-0857-2026 · Official record ↗

FDA Class II · Drug · September 30, 2026

Reliable -1 Laboratories recall — Sterling Pharmaceutical Services LLC

Lack of Assurance of Sterility

Company / brand: Sterling Pharmaceutical Services recalls

Official ID D-0856-2026 · Official record ↗

FDA Class II · Drug · September 30, 2026

AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0 recall — Sterling Pharmaceutical Services LLC

Lack of Assurance of Sterility

Company / brand: Sterling Pharmaceutical Services recalls

Official ID D-0855-2026 · Official record ↗

FDA Class II · Drug · September 30, 2026

MENOW SUNSCREEN PRESSED POWDER SPF35 PA+++ recall — SHANTOU Qiwei industrial Co., Ltd

cGMP Deviations

Company / brand: SHANTOU Qiwei industrial Co recalls

Official ID D-0854-2026 · Official record ↗

FDA Not Yet Classified · Drug · September 23, 2026

Nystatin Cream recall — SUN PHARMACEUTICAL INDUSTRIES INC

Failed Stability Specifications

Company / brand: SUN PHARMACEUTICAL INDUSTRIES recalls

Official ID EVT-99876-z42zg7 · Official record ↗

FDA Not Yet Classified · Food · September 23, 2026

Heinz Real - Vraie Mayonnaise recall — KRAFT HEINZ FOODS COMPANY

undeclared ingredients including but not limited to mustard

Company / brand: KRAFT HEINZ FOODS COMPANY recalls

Official ID EVT-99869-14pecqd · Official record ↗

FDA Class II · Medical device · September 23, 2026

Pi-Cardia Inc recall — PI CARDIA LTD

Transfemoral catheter, positing arm may detached due to weld issue.

Company / brand: PI CARDIA recalls

Official ID Z-3213-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

CADD Yellow Medication Cassette Reservoir with NRFit connector US Product Codes recall — ICU Medical, Inc.

Reservoirs may exhibit medication leakage at the joint between luer connector and tubing. Issue could result in delay or interruption of therapy, under delivery of medication, expo…

Company / brand: ICU Medical recalls

Official ID Z-3212-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Reign Medical Clench Staple System (Compression) recall — F & A Foundation

Bone fixation staple requires a new 510(k); the performance characteristics of this device have not been adequately established.

Company / brand: F & A Foundation recalls

Official ID Z-3211-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Convenience kits CATARACT PACK DYNJ59881A recall — Medline Industries, LP

Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field o…

Company / brand: Medline Industries recalls

Official ID Z-3210-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Convenience kits MYRINGOTOMY PACK-LF DYNJ59097A recall — Medline Industries, LP

Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field o…

Company / brand: Medline Industries recalls

Official ID Z-3209-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Convenience kits MINOR PACK DYNJ58421A SPRINGHILL MINOR PACK DYNJ40734F recall — Medline Industries, LP

Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field o…

Company / brand: Medline Industries recalls

Official ID Z-3208-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A recall — Medline Industries, LP

Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field o…

Company / brand: Medline Industries recalls

Official ID Z-3207-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

SCORPIO C-DOME PATELLA 73-2710 73-2910 SCORPIO U-DOME PATELLA 73-3110 73-3508 73-3708 73-3 recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Company / brand: Howmedica Osteonics recalls

Official ID Z-3206-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

SCORPIO + MOBILE BEARING PCS 78-5-0910 SYSTEM ONE BIPOLAR 40MM 6074-4022 SYSTEM ONE BIPOLA recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Company / brand: Howmedica Osteonics recalls

Official ID Z-3205-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

TRIDENT 0¿ POLY INSERT 28mm ID 620-00-28D Orthopaedic implant components manufactured from recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Company / brand: Howmedica Osteonics recalls

Official ID Z-3204-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

SCORPIO RECESSED METAL BACKED PATELLA 3045-0026 3045-0028 3045-0030 3045-0032 Orthopaedic recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Company / brand: Howmedica Osteonics recalls

Official ID Z-3203-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

BEARING AND AXLE BUSHING ASSY STD ELBOW C-M113-1-301 KRH REV TIB INS 16mm THK recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Company / brand: Howmedica Osteonics recalls

Official ID Z-3202-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

ACETABULAR CUP UHMWPE 61-3258 ALL POLY CONSTRAINED INSERT 44MM 69-2244 ALL POLY CONSTRAINE recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Company / brand: Howmedica Osteonics recalls

Official ID Z-3201-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

DURACON XL ANGLED TIB INS 11/14MM C-M064-1-300 SELF-PRESSURIZING GLENOID SIZE 8 C-M062-6-8 recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Company / brand: Howmedica Osteonics recalls

Official ID Z-3200-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

ABG I ACETABULAR INSERT HOODED 28mm ID X 48mm C-M079-2-801 ARC2F ACETABULAR INSERT 48/50/5 recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Company / brand: Howmedica Osteonics recalls

Official ID Z-3199-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

TRIATHLON HINGE INSERT SIZE 4 11MM 5612-P-411 TRIATHLON HINGE INSERT SIZE 4 13MM 5612-P-41 recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Company / brand: Howmedica Osteonics recalls

Official ID Z-3198-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

ALL POLY CONSTRAINED INSERT 54MM 69-2854 NRG KNEE CR 82-2-0512 82-2-0518 82-2-0912 NRG KNE recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Company / brand: Howmedica Osteonics recalls

Official ID Z-3197-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

OMNIFIT SERIES I ACET recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Company / brand: Howmedica Osteonics recalls

Official ID Z-3196-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

AXLE PIN ASSY LARGE ELBOW COBALT CHROME Catalog No recall — Howmedica Osteonics Corp.

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o…

Company / brand: Howmedica Osteonics recalls

Official ID Z-3195-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Captus 4000e Thyroid Uptake System recall — Mirion Technologies (Capintec), Inc.

Potential for failure of the tension bolt which would allow the spring arm to unexpectedly fall to its lowest position, which is approximately 25 inches (63.5 cm) from the ground.

Company / brand: Mirion Technologies (Capintec) recalls

Official ID Z-3193-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Et Control recall — Datex-Ohmeda, Inc.

Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control, the system delivers 10…

Company / brand: Datex-Ohmeda recalls

Official ID Z-3192-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Aisys CS2 with Et Control recall — Datex-Ohmeda, Inc.

Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control, the system delivers 10…

Company / brand: Datex-Ohmeda recalls

Official ID Z-3191-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Aisys CS2 recall — Datex-Ohmeda, Inc.

Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control, the system delivers 10…

Company / brand: Datex-Ohmeda recalls

Official ID Z-3190-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Aisys recall — Datex-Ohmeda, Inc.

Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control, the system delivers 10…

Company / brand: Datex-Ohmeda recalls

Official ID Z-3189-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Boston Scientific Corporation StoneSmart Connect Console Contents recall — Boston Scientific Corporation

A subset of power adapters used with the connect console may exhibit higher-than-expected resistance in the electrical grounding path. As a result, the power adaptor may fail elect…

Company / brand: Boston Scientific recalls

Official ID Z-3188-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

REF recall — Stryker Sustainability Solutions

Reusable access port system may crack or seperate during use.

Company / brand: Stryker Sustainability Solutions recalls

Official ID Z-3187-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

REF recall — Stryker Sustainability Solutions

Reusable access port system may crack or seperate during use.

Company / brand: Stryker Sustainability Solutions recalls

Official ID Z-3186-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

REF recall — Stryker Sustainability Solutions

Reusable access port system may crack or seperate during use.

Company / brand: Stryker Sustainability Solutions recalls

Official ID Z-3185-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

REF recall — Stryker Sustainability Solutions

Reusable access port system may crack or seperate during use.

Company / brand: Stryker Sustainability Solutions recalls

Official ID Z-3184-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

REF recall — Stryker Sustainability Solutions

Reusable access port system may crack or seperate during use.

Company / brand: Stryker Sustainability Solutions recalls

Official ID Z-3183-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

REF recall — Stryker Sustainability Solutions

Reusable access port system may crack or seperate during use.

Company / brand: Stryker Sustainability Solutions recalls

Official ID Z-3182-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Blood Culture Collection Venipuncture Kit 20/Cs recall — Medical Action Industries, Inc. 306

Blood culture convenience kits contain a component subject to a drug recall that due to an an open or incomplete seal on the packaging of the applicator may compromise the componen…

Company / brand: Medical Action Industries recalls

Official ID Z-3181-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

EWO_02513 (Catalog number 320122) For Investigational Use Only Nano Un-Cannulated Demo Sam recall — embecta Medical II LLC

Retrospectively reported: Pen needles labeled 'For Investigational Use Only' were inadvertently distributed as commercially marketed devices.

Company / brand: embecta Medical II recalls

Official ID Z-3180-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

EWO_02512 (Catalog number 320550) For Investigational Use Only Nano Pro Un-Cannulated Demo recall — embecta Medical II LLC

Retrospectively reported: Pen needles labeled 'For Investigational Use Only' were inadvertently distributed as commercially marketed devices.

Company / brand: embecta Medical II recalls

Official ID Z-3179-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Kinos Axiom Total Ankle System with Axiom PSR recall — restor3d Inc.

Ankle implantation systems were packaged with incorrect patient-specific cutting guides, which may result in: delayed surgery, the need to use standard instrumentation, reduced fix…

Company / brand: restor3d recalls

Official ID Z-3178-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Brand Name recall — Wilson-Cook Medical Inc.

Due to issue with endoscope adherence and inability to spray powder. Firm will provide an updated Instruction for Use (IFU).

Company / brand: Wilson-Cook Medical recalls

Official ID Z-3177-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Happiest Baby recall — Happiest Baby, Inc

Extra small (ES) and Extra-large (XL) infant sleep sacks have not been reviewed for safety and effectiveness by the FDA.

Company / brand: Happiest Baby recalls

Official ID Z-3176-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Happiest Baby recall — Happiest Baby, Inc

Extra small (ES) and Extra-large (XL) infant sleep sacks have not been reviewed for safety and effectiveness by the FDA.

Company / brand: Happiest Baby recalls

Official ID Z-3175-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Brand Name recall — PTW FREIBURG

When a bolus is included in a treatment plan and sent for secondary dose calculation, the software accounts for it but does not display this clearly, which may lead users to incorr…

Company / brand: PTW FREIBURG recalls

Official ID Z-3174-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

GM Helix Implant recall — Straumann USA LLC

There is a discrepancy between the product identification on the packaging and the dimensions of the implant contained inside.

Company / brand: Straumann USA recalls

Official ID Z-3173-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

SunMed Tracheal Tube recall — WELL LEAD MEDICAL CO. LTD

The 6Fr suction catheter could not pass through the samples smoothly.

Company / brand: WELL LEAD MEDICAL CO recalls

Official ID Z-3172-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Core Services Hub V8 recall — GE Healthcare

Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be …

Company / brand: GE Healthcare recalls

Official ID Z-3171-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Workflow Core Services V8 recall — GE Healthcare

Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be …

Company / brand: GE Healthcare recalls

Official ID Z-3170-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Centricity PACS Server V7 recall — GE Healthcare

Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be …

Company / brand: GE Healthcare recalls

Official ID Z-3169-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Centricity PACS V2 recall — GE Healthcare

Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be …

Company / brand: GE Healthcare recalls

Official ID Z-3168-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Enterprise Archive V8 recall — GE Healthcare

Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be …

Company / brand: GE Healthcare recalls

Official ID Z-3167-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Centricity Enterprise Archive V2 recall — GE Healthcare

Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be …

Company / brand: GE Healthcare recalls

Official ID Z-3166-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

NOxBOXi Nitric Oxide Delivery System recall — NOXBOX LTD

Potential for oxygen tubing leaks due to failure of the tubing or tubing connection, which may lead to oxygen desaturation.

Company / brand: NOXBOX recalls

Official ID Z-3165-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Brand Name recall — Nuclein LLC

Due to a software issue

Company / brand: Nuclein recalls

Official ID Z-3164-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

IV Sets with drip chambers recall — ICU Medical, Inc.

Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…

Company / brand: ICU Medical recalls

Official ID Z-3163-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

IV Sets with drip chambers recall — ICU Medical, Inc.

Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…

Company / brand: ICU Medical recalls

Official ID Z-3162-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

IV Sets with drip chambers recall — ICU Medical, Inc.

Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…

Company / brand: ICU Medical recalls

Official ID Z-3161-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

IV Sets with drip chambers recall — ICU Medical, Inc.

Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…

Company / brand: ICU Medical recalls

Official ID Z-3160-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Oncology sets with drip chambers recall — ICU Medical, Inc.

Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…

Company / brand: ICU Medical recalls

Official ID Z-3159-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Oncology sets with drip chambers recall — ICU Medical, Inc.

Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…

Company / brand: ICU Medical recalls

Official ID Z-3158-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

IV Non-Dedicated Gravity Administration Sets with drip chambers recall — ICU Medical, Inc.

Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…

Company / brand: ICU Medical recalls

Official ID Z-3157-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Plum administration sets recall — ICU Medical, Inc.

Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material with…

Company / brand: ICU Medical recalls

Official ID Z-3156-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Haylard UNIV IMAGING BIOPSY TRUCUSTOM recall — AVID Medical, Inc.

Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.

Company / brand: AVID Medical recalls

Official ID Z-3154-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Haylard BASIC BIOPSY TRAY recall — AVID Medical, Inc.

Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.

Company / brand: AVID Medical recalls

Official ID Z-3153-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Haylard CONTINUOUS NERVE BLOCK TRAY recall — AVID Medical, Inc.

Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.

Company / brand: AVID Medical recalls

Official ID Z-3152-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Haylard 18G SINGLE SHOT EPI TRAY recall — AVID Medical, Inc.

Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.

Company / brand: AVID Medical recalls

Official ID Z-3151-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Impella Optical Controller recall — Abiomed, Inc.

The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly.

Company / brand: Abiomed recalls

Official ID Z-3150-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Impella Optical Controller with the below product descriptions and corresponding Product C recall — Abiomed, Inc.

The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly.

Company / brand: Abiomed recalls

Official ID Z-3149-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Automated Impella Controller (AIC) with the below product descriptions and corresponding P recall — Abiomed, Inc.

The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly.

Company / brand: Abiomed recalls

Official ID Z-3148-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

MEDRAD¿ Stellant FLEX Syringe Kit used with Stellant FLEX CT Injection System recall — Bayer Medical Care, Inc.

Some devices may not have been properly sterilized due to a manufacturing sterilization issue.

Company / brand: Bayer Medical Care recalls

Official ID Z-3147-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Percutaneous Insertion Kit (PIK) recall — Maquet Cardiopulmonary Gmbh

The packaging may not consistently maintain sterile barrier integrity.

Company / brand: Maquet Cardiopulmonary recalls

Official ID Z-3146-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Percutaneous Insertion Kit (PIK) recall — Maquet Cardiopulmonary Gmbh

The packaging may not consistently maintain sterile barrier integrity.

Company / brand: Maquet Cardiopulmonary recalls

Official ID Z-3145-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Percutaneous Insertion Kit (PIK) recall — Maquet Cardiopulmonary Gmbh

The packaging may not consistently maintain sterile barrier integrity.

Company / brand: Maquet Cardiopulmonary recalls

Official ID Z-3144-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04 recall — GE Medical Systems Information Technologies Inc

Device may not resume patient monitoring for at least 3 minutes following system restart. Issue can lead to potential delay in recognition of clinically significant events.

Company / brand: GE Medical Systems Information Technologies recalls

Official ID Z-3143-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Philips PIC iX Essentials REF recall — Philips North America

Due to software malfunction, patient information system may freeze and become unresponsive.

Company / brand: Philips North America recalls

Official ID Z-3142-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Philips Patient Information Center iX REF recall — Philips North America

Due to software malfunction, patient information system may freeze and become unresponsive.

Company / brand: Philips North America recalls

Official ID Z-3141-2026 · Official record ↗

FDA Class II · Medical device · September 23, 2026

Medline Convenience Kit recall — Medline Industries, LP

The kits contain a Retrograde Coronary Sinus Perfusion (RCSP) cannulae that has the potential for a sterile barrier breach. Sterility of the product cannot be assured. If a comprom…

Company / brand: Medline Industries recalls

Official ID Z-3137-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

StatStrip Glucose and B- Ketone meter recall — Nova Biomedical Corporation

A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a previously scanned barcode i…

Company / brand: Nova Biomedical recalls

Official ID Z-3132-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

StatStrip Glucose and B- Ketone meter recall — Nova Biomedical Corporation

A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a previously scanned barcode i…

Company / brand: Nova Biomedical recalls

Official ID Z-3131-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

StatStrip Glucose and B- Ketone meter recall — Nova Biomedical Corporation

A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a previously scanned barcode i…

Company / brand: Nova Biomedical recalls

Official ID Z-3130-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

StatStrip Glucose Hospital Meter System recall — Nova Biomedical Corporation

A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a previously scanned barcode i…

Company / brand: Nova Biomedical recalls

Official ID Z-3129-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

StatStrip Glucose Hospital Meter System recall — Nova Biomedical Corporation

A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a previously scanned barcode i…

Company / brand: Nova Biomedical recalls

Official ID Z-3128-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillu…

Company / brand: Medline Industries recalls

Official ID Z-3127-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillu…

Company / brand: Medline Industries recalls

Official ID Z-3126-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillu…

Company / brand: Medline Industries recalls

Official ID Z-3125-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillu…

Company / brand: Medline Industries recalls

Official ID Z-3124-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillu…

Company / brand: Medline Industries recalls

Official ID Z-3123-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillu…

Company / brand: Medline Industries recalls

Official ID Z-3122-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillu…

Company / brand: Medline Industries recalls

Official ID Z-3121-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Halyard IV START KIT NON-STERILE REF recall — AVID Medical, Inc.

Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which are contaminated with Aspergillus penicillioides

Company / brand: AVID Medical recalls

Official ID Z-3108-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusi recall — BD SWITZERLAND SARL

Due to discrepancies in specific attributes in the performance data for infusion sets, which may lead to inappropriate pump performance.

Company / brand: BD SWITZERLAND SARL recalls

Official ID Z-3080-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

DuoGlide Short-Term Straight Dialysis Catheter recall — Bard Access Systems, Inc.

this is a downstream recall of class I recall RES 98777

Company / brand: Bard Access Systems recalls

Official ID Z-2985-2026 · Official record ↗

FDA Class I · Medical device · September 23, 2026

Power-Trialysis Short-Term Straight Dialysis Catheter recall — Bard Access Systems, Inc.

this is a downstream recall of class I recall RES 98777

Company / brand: Bard Access Systems recalls

Official ID Z-2984-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Mon Sire Brie recall — Optimus Inc. d/b/a/ Markys Caviar

The firm was notified by their Brie Cheese supplier that sample results revealed the presence of Listeria monocytogenes.

Company / brand: Optimus d/b/a/ Markys Caviar recalls

Official ID H-1388-2026 · Official record ↗

FDA Class III · Food · September 23, 2026

Hexing Haw Balls candy recall — Tiffany Food Corp

Unapproved dye Ponceau 4R

Company / brand: Tiffany Food recalls

Official ID H-1387-2026 · Official record ↗

FDA Class II · Food · September 23, 2026

PUMPKIN SPICE NO BAKE COOKIE NET WT 3 recall — Best Friends Bakery, LLC

Peanuts & Eggs. The firm list peanuts in the ingredient statement but omitted them from the contain statement. They also have eggs listed in the contain statement but there are no …

Company / brand: Best Friends Bakery recalls

Official ID H-1386-2026 · Official record ↗

FDA Class II · Food · September 23, 2026

Elegant Foods Carrot Cake recall — Elegant Foods, LLC

Carrot decoration contains Yellow #5 and Yellow #6 which is not listed on finished product label.

Company / brand: Elegant Foods recalls

Official ID H-1385-2026 · Official record ↗

FDA Class II · Food · September 23, 2026

Elegant Foods Golden Raisins recall — Elegant Foods, LLC

Undeclared sulfites

Company / brand: Elegant Foods recalls

Official ID H-1384-2026 · Official record ↗

FDA Class II · Food · September 23, 2026

Elegant Foods Coconut Flakes recall — Elegant Foods, LLC

Undeclared sulfites

Company / brand: Elegant Foods recalls

Official ID H-1383-2026 · Official record ↗

FDA Class II · Food · September 23, 2026

Buckhead recall — Buckhead Meat Company D.B.A. Trinity Seafood

The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.

Company / brand: Buckhead Meat Company D.B.A. Trinity Seafood recalls

Official ID H-1382-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Organic Triple Berry Blend Strawberries recall — Frutas y Hortalizas del Sur S.A.

Potential E. coli O145:H28 Contamination

Company / brand: Frutas y Hortalizas del Sur recalls

Official ID H-1380-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

PICO DE GALLO-HOT-6/9oz HEB-PICO-HOT-12/14oz recall — NatureBest Pre-Cut & Produce LLc

Jalapenos have the potential to be contaminated with Salmonella

Company / brand: NatureBest Pre-Cut & Produce recalls

Official ID H-1379-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

HEB-PICO-MEDIUM-12/14oz PICO DE GALLO-MEDIUM-6/14oz PICO DE GALLO-MEDIUM-6/9oz PICO-DE-GAL recall — NatureBest Pre-Cut & Produce LLc

Jalapenos have the potential to be contaminated with Salmonella

Company / brand: NatureBest Pre-Cut & Produce recalls

Official ID H-1378-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

HEB-GUAC KIT-MILD-3/57 recall — NatureBest Pre-Cut & Produce LLc

Jalapenos have the potential to be contaminated with Salmonella

Company / brand: NatureBest Pre-Cut & Produce recalls

Official ID H-1377-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

NatureBest Mild Cheddar & Jalapeno Stuffed Mushrooms 8oz (227g) HEB SI JAL POP STFFD MUSHR recall — NatureBest Pre-Cut & Produce LLc

Jalapenos have the potential to be contaminated with Salmonella

Company / brand: NatureBest Pre-Cut & Produce recalls

Official ID H-1376-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

PEPPER-JALAPENO-DC 1/4"-4/5# PEPPER-JALAPENO-DC 1/4"-1/5# PEPPER-JALAPENO-SL 1/8"-1/5# PEP recall — NatureBest Pre-Cut & Produce LLc

Jalapenos have the potential to be contaminated with Salmonella

Company / brand: NatureBest Pre-Cut & Produce recalls

Official ID H-1375-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

HEB-PICO-MANGO-12/14oz PICO DE GALLO-MANGO-4/14oz PICO DE GALLO-MANGO-6/14oz recall — NatureBest Pre-Cut & Produce LLc

Jalapenos have the potential to be contaminated with Salmonella

Company / brand: NatureBest Pre-Cut & Produce recalls

Official ID H-1374-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

SOUP MIX-6/58oz Tray recall — NatureBest Pre-Cut & Produce LLc

Jalapenos have the potential to be contaminated with Salmonella

Company / brand: NatureBest Pre-Cut & Produce recalls

Official ID H-1373-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

PICO DE GALLO-MILD-4oz PICO DE GALLO-MILD-6/14oz PICO DE GALLO-4/5# PICO DE GALLO-1/5# PIC recall — NatureBest Pre-Cut & Produce LLc

Jalapenos have the potential to be contaminated with Salmonella

Company / brand: NatureBest Pre-Cut & Produce recalls

Official ID H-1372-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

BH Bold Chef Salad Kit recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1368-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Pico De Gallo recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1367-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Fresh Pico Tray recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1366-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Pico De Gallo Hot recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1365-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Tomato Salsa Fresca recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1364-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Salsa Fresca Medium recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1363-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Salsa Verde Mild recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1362-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Salsa Roja Medium recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1361-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Pico De Gallo Spicy recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1360-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Pico De Gallo Mild recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1359-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Hot Pico De Gallo recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1358-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Mild Pico De Gallo recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1357-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Pico De Gallo recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1356-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Pico De Gallo recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1355-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Pineapple Mango Salsa Mild recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1354-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Mango Pico De Gallo recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1353-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Authentic Guacamole recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1352-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Spicy Guacamole recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1351-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Fiesta Salad with Shrimp recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1350-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Taco Dip recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1349-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Spicy Pimento Cheese Dip recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1348-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Spicy Jalapeno Jarlsberg Dip recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1347-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Spicy Roast Beef Sandwich (closed-face) recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1346-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Rice & Bean Burrito recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1345-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Diced Jalapenos recall — Taylor Fresh Foods Inc

Potential contamination with Salmonella.

Company / brand: Taylor Fresh Foods recalls

Official ID H-1344-2026 · Official record ↗

FDA Class II · Food · September 23, 2026

Mercer's brand 6 ICE CREAM SANDWICHES TO GO recall — Quality Dairy Farms Inc.

Undeclared peanuts

Company / brand: Quality Dairy Farms recalls

Official ID H-1343-2026 · Official record ↗

FDA Class II · Food · September 23, 2026

Martina brand Fresh Whole Mangoes recall — Panorama Produce Sales Inc.

Product may be contaminated with Salmonella

Company / brand: Panorama Produce Sales recalls

Official ID H-1342-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Everything Sprouts Robust Radish Mix recall — Everything Sprouts, LLC

Sprouts may be contaminated with STEC E. coli and/or Salmonella.

Company / brand: Everything Sprouts recalls

Official ID H-1340-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Everything Sprouts Crunchy Protein Sprout Mix recall — Everything Sprouts, LLC

Sprouts may be contaminated with STEC E. coli and/or Salmonella.

Company / brand: Everything Sprouts recalls

Official ID H-1339-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Everything Sprouts Zesty Garlic Mix recall — Everything Sprouts, LLC

Sprouts may be contaminated with STEC E. coli and/or Salmonella.

Company / brand: Everything Sprouts recalls

Official ID H-1338-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Everything Sprouts and Calco branded Alfalfa Sprouts recall — Everything Sprouts, LLC

Sprouts may be contaminated with STEC E. coli and/or Salmonella.

Company / brand: Everything Sprouts recalls

Official ID H-1337-2026 · Official record ↗

FDA Class I · Food · September 23, 2026

Foods Alive organic moringa leaf powder recall — FOODS ALIVE INC.

Potential Salmonella contamination

Company / brand: FOODS ALIVE recalls

Official ID H-1336-2026 · Official record ↗

FDA Class I · Drug · September 23, 2026

Thyroid Tablets recall — VITRUVIAS THERAPEUTICS INC

Superpotent Drug

Company / brand: VITRUVIAS THERAPEUTICS recalls

Official ID D-0866-2026 · Official record ↗

FDA Class II · Drug · September 23, 2026

Dopamine HCl Inj recall — Pfizer

Lack of Assurance of Sterility

Company / brand: Pfizer recalls

Official ID D-0853-2026 · Official record ↗

FDA Class II · Drug · September 23, 2026

Chlorthalidone Tablets recall — Inventia Healthcare Limited

Failed Dissolution Specifications

Company / brand: Inventia Healthcare recalls

Official ID D-0852-2026 · Official record ↗

FDA Class II · Drug · September 23, 2026

Lidocaine Ointment USP recall — SUN PHARMA /TARO

Failed Content Uniformity Specifications. Out of Specification for Assay during analysis at the 24- month long term stability station, at (25¿C,60%RH).

Company / brand: SUN PHARMA /TARO recalls

Official ID D-0848-2026 · Official record ↗

FDA Class II · Drug · September 23, 2026

Fluphenazine HCl Elixir recall — Safecor Health, LLC

Failed Stability Specifications

Company / brand: Safecor Health recalls

Official ID D-0846-2026 · Official record ↗

FDA Class II · Drug · September 23, 2026

Fluphenazine HCl Elixir recall — Safecor Health, LLC

Failed Stability Specifications

Company / brand: Safecor Health recalls

Official ID D-0845-2026 · Official record ↗

FDA Class II · Drug · September 23, 2026

Fluphenazine HCl Elixir recall — Safecor Health, LLC

Failed Stability Specifications

Company / brand: Safecor Health recalls

Official ID D-0844-2026 · Official record ↗

FDA Class II · Drug · September 23, 2026

Fluphenazine HCl Elixir recall — Safecor Health, LLC

Failed Stability Specifications

Company / brand: Safecor Health recalls

Official ID D-0843-2026 · Official record ↗

FDA Class II · Drug · September 23, 2026

Fluphenazine HCl Elixir recall — Safecor Health, LLC

Failed Stability Specifications

Company / brand: Safecor Health recalls

Official ID D-0842-2026 · Official record ↗

FDA Class II · Drug · September 23, 2026

Fluphenazine HCl Elixir recall — Safecor Health, LLC

Failed Stability Specifications

Company / brand: Safecor Health recalls

Official ID D-0841-2026 · Official record ↗

FDA Not Yet Classified · Drug · September 16, 2026

fentaNYL Citrate recall — OurPharma LLC

Labeling: Not Elsewhere Classified: Complaint received on 08/31/2026 regarding the discrepancy of the IV bag expiry (07/31/2026 and 11/30/2026) and the product expiry (12/09/2026).

Company / brand: OurPharma recalls

Official ID EVT-99837-1lubpwm · Official record ↗

FDA Class II · Medical device · September 16, 2026

AMS Convenience Kit recall — Windstone Medical Packaging, Inc.

The convenience kits contain .0.9% Sodium Chloride Injection, USP products in Single Dose freeflex bags, which may contain blue Break-off-Parts (BOPs) that have detached from the i…

Company / brand: Windstone Medical Packaging recalls

Official ID Z-3138-2026 · Official record ↗

FDA Class II · Medical device · September 16, 2026

Citric Complete Liquid Citric Acid Concentrate REF recall — Nipro Renal Soultions USA, Corporation

Hemodialysis concentrates contain high endotoxin levels

Company / brand: Nipro Renal Soultions USA recalls

Official ID Z-3136-2026 · Official record ↗

FDA Class II · Medical device · September 16, 2026

Citric Complete Dry Citric Acid Concentrate REF recall — Nipro Renal Soultions USA, Corporation

Hemodialysis concentrates contain high endotoxin levels

Company / brand: Nipro Renal Soultions USA recalls

Official ID Z-3135-2026 · Official record ↗

FDA Class II · Medical device · September 16, 2026

MedicaLyte Bicarbonate Powder REF recall — Nipro Renal Soultions USA, Corporation

Hemodialysis concentrates contain high endotoxin levels

Company / brand: Nipro Renal Soultions USA recalls

Official ID Z-3134-2026 · Official record ↗

FDA Class II · Medical device · September 16, 2026

MedicaLyte Liquid Bicarbonate Concentrate REF recall — Nipro Renal Soultions USA, Corporation

Hemodialysis concentrates contain high endotoxin levels

Company / brand: Nipro Renal Soultions USA recalls

Official ID Z-3133-2026 · Official record ↗

FDA Class II · Medical device · September 16, 2026

HeartSine SAM 350P 350P US Device recall — HeartSine Technologies Ltd

Due to a damaged (over stretched) membrane tail that causes an intermittent fault.

Company / brand: HeartSine Technologies recalls

Official ID Z-3120-2026 · Official record ↗

FDA Class II · Medical device · September 16, 2026

Products that contain the Pericare Wipes recall — C.R. Bard Inc

Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

Company / brand: C.R. Bard recalls

Official ID Z-3119-2026 · Official record ↗

FDA Class II · Medical device · September 16, 2026

Products that contain the Pericare Wipes recall — C.R. Bard Inc

Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

Company / brand: C.R. Bard recalls

Official ID Z-3118-2026 · Official record ↗

FDA Class II · Medical device · September 16, 2026

Products that contain the Pericare Wipes recall — C.R. Bard Inc

Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

Company / brand: C.R. Bard recalls

Official ID Z-3117-2026 · Official record ↗

FDA Class II · Medical device · September 16, 2026

Products that contain the Pericare Wipes recall — C.R. Bard Inc

Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

Company / brand: C.R. Bard recalls

Official ID Z-3116-2026 · Official record ↗

FDA Class II · Medical device · September 16, 2026

Products that contain the Pericare Wipes recall — C.R. Bard Inc

Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

Company / brand: C.R. Bard recalls

Official ID Z-3115-2026 · Official record ↗

FDA Class II · Medical device · September 16, 2026

Products that contain the Pericare Wipes recall — C.R. Bard Inc

Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

Company / brand: C.R. Bard recalls

Official ID Z-3114-2026 · Official record ↗

FDA Class II · Medical device · September 16, 2026

Getinge PVC Thoracic Catheter recall — Atrium Medical Corporation

An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters.

Company / brand: Atrium Medical recalls

Official ID Z-3113-2026 · Official record ↗

FDA Class II · Medical device · September 16, 2026

Getinge PVC Thoracic Catheter recall — Atrium Medical Corporation

An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters.

Company / brand: Atrium Medical recalls

Official ID Z-3112-2026 · Official record ↗

FDA Class II · Medical device · September 16, 2026

Getinge PVC Thoracic Catheter recall — Atrium Medical Corporation

An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters.

Company / brand: Atrium Medical recalls

Official ID Z-3111-2026 · Official record ↗

FDA Class II · Medical device · September 16, 2026

Product Name recall — Lutronic Corporation

Utilizing higher fluences at 1064nm wavelength with current cryogen parameters may result in a spark/loud noise during treatment, potentially resulting in patient burn.

Company / brand: Lutronic recalls

Official ID Z-3110-2026 · Official record ↗

FDA Class II · Medical device · September 16, 2026

Halyard IV Start Kit Non-Sterile REF recall — AVID Medical, Inc.

Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper lidding which may breach the …

Company / brand: AVID Medical recalls

Official ID Z-3109-2026 · Official record ↗

FDA Class I · Medical device · September 16, 2026

Kit recall — Medical Action Industries, Inc. 306

Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.

Company / brand: Medical Action Industries recalls

Official ID Z-3107-2026 · Official record ↗

FDA Class I · Medical device · September 16, 2026

Kit recall — Medical Action Industries, Inc. 306

Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.

Company / brand: Medical Action Industries recalls

Official ID Z-3106-2026 · Official record ↗

FDA Class I · Medical device · September 16, 2026

Bravo CF capsule delivery device recall — Given Imaging Ltd.

Capsule may fail to attach to the esophagus or detach from the delivery device. Risks include patient aspiration/inhalation, perforation of esophagus, obstruction of the airway, he…

Company / brand: Given Imaging recalls

Official ID Z-3090-2026 · Official record ↗

FDA Class I · Food · September 16, 2026

Alfalfa recall — International Sprout Holdings, Inc

Potential E. coli and Salmonella contamination

Company / brand: International Sprout Holdings recalls

Official ID H-1341-2026 · Official record ↗

FDA Class II · Food · September 16, 2026

Prolon Everyday Apulian Almond & Cocoa Spread recall — L-Nutra Inc

Undeclared allergen (tree nuts): hazelnut, cashew, and pistachio.

Company / brand: L-Nutra recalls

Official ID H-1335-2026 · Official record ↗

FDA Class II · Food · September 16, 2026

Fannie May & XO Marshmallow Pixie S'mores Collection recall — Ferrero USA

Undeclared milk and pecans

Company / brand: Ferrero USA recalls

Official ID H-1334-2026 · Official record ↗

FDA Class I · Food · September 16, 2026

Crown Farms Dried Suri Cut recall — EURO FOODS GROUP USA NJ INC

The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying.

Company / brand: EURO FOODS GROUP USA NJ recalls

Official ID H-1331-2026 · Official record ↗

FDA Class I · Food · September 16, 2026

Momchipz Gluten Free Veggie Chips Broccoli Florets & Cauliflower recall — EXOTIQUE FOODS CANADA

Undeclared Wheat.

Company / brand: EXOTIQUE FOODS CANADA recalls

Official ID H-1330-2026 · Official record ↗

FDA Class I · Drug · September 16, 2026

0 recall — B BRAUN MEDICAL INC

Presence of Particulate Matter: particulate matter identified as iron oxide, inorganic material, cellulose cotton fiber or polystyrene

Company / brand: B BRAUN MEDICAL recalls

Official ID D-0869-2026 · Official record ↗

FDA Class I · Drug · September 16, 2026

Epinephrine Injection recall — American Regent, Inc.

Presence of Particulate Matter and Lack of Assurance of Sterility. Particulate matter identified as nylon, cellulosic, acrylic, polyethylene and glass and broken and leaking vials.

Company / brand: American Regent recalls

Official ID D-0865-2026 · Official record ↗

FDA Class II · Drug · September 16, 2026

fentaNYL Citrate recall — OurPharma LLC

Labeling: Not Elsewhere Classified: Complaint received on 08/31/2026 regarding the discrepancy of the IV bag expiry (07/31/2026 and 11/30/2026) and the product expiry (12/09/2026).

Company / brand: OurPharma recalls

Official ID D-0864-2026 · Official record ↗

FDA Class I · Drug · September 16, 2026

Dextrose Injection recall — Baxter Healthcare Corporation

Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution.

Company / brand: Baxter Healthcare recalls

Official ID D-0850-2026 · Official record ↗

FDA Class III · Drug · September 16, 2026

Fluphenazine Hydrochloride Tablets recall — Ajanta Pharma USA Inc

Failed impurities/degradation specifications: (OOS) for Organic Impurities by HPLC (Impurity-A) during testing at the 18 months long term stability. Result: 1.1 percent. Spec: 1.0 …

Company / brand: Ajanta Pharma USA recalls

Official ID D-0836-2026 · Official record ↗

FDA Class III · Drug · September 16, 2026

Povidone Iodine 1 recall — ImprimisRx NJ LLC

Subpotent Drug

Company / brand: ImprimisRx NJ recalls

Official ID D-0835-2026 · Official record ↗

FDA Not Yet Classified · Drug · September 9, 2026

Prasugrel HCI recall — Golden State Medical Supply Inc.

Failed Dissolution Specifications. Notification from the manufacturer that lot is being recalled due to failed dissolution

Company / brand: Golden State Medical Supply recalls

Official ID EVT-99732-3aiyt7 · Official record ↗

FDA Class I · Food · September 9, 2026

Food to Live Organic SuperGrass Powder recall — Lexunder Inc

Contaminated with Salmonella

Company / brand: Lexunder recalls

Official ID EVT-99582-2r09zi · Official record ↗

FDA Class II · Medical device · September 9, 2026

Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays recall — Cardinal Health 200, LLC

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…

Company / brand: Cardinal Health 200 recalls

Official ID Z-3105-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays recall — Cardinal Health 200, LLC

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…

Company / brand: Cardinal Health 200 recalls

Official ID Z-3104-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays recall — Cardinal Health 200, LLC

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…

Company / brand: Cardinal Health 200 recalls

Official ID Z-3103-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays recall — Cardinal Health 200, LLC

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…

Company / brand: Cardinal Health 200 recalls

Official ID Z-3102-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays recall — Cardinal Health 200, LLC

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…

Company / brand: Cardinal Health 200 recalls

Official ID Z-3101-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays recall — Cardinal Health 200, LLC

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…

Company / brand: Cardinal Health 200 recalls

Official ID Z-3100-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays recall — Cardinal Health 200, LLC

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…

Company / brand: Cardinal Health 200 recalls

Official ID Z-3099-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays recall — Cardinal Health 200, LLC

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…

Company / brand: Cardinal Health 200 recalls

Official ID Z-3098-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays recall — Cardinal Health 200, LLC

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…

Company / brand: Cardinal Health 200 recalls

Official ID Z-3097-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays recall — Cardinal Health 200, LLC

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…

Company / brand: Cardinal Health 200 recalls

Official ID Z-3096-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays recall — Cardinal Health 200, LLC

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…

Company / brand: Cardinal Health 200 recalls

Official ID Z-3095-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays recall — Cardinal Health 200, LLC

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…

Company / brand: Cardinal Health 200 recalls

Official ID Z-3094-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Citrasate recall — Fresenius Medical Care Renal Therapies Group, LLC

Complaints of blue-green discoloration in product

Company / brand: Fresenius Medical Care Renal Therapies Group recalls

Official ID Z-3093-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

NaturaLyte recall — Fresenius Medical Care Renal Therapies Group, LLC

Complaints of blue-green discoloration in product

Company / brand: Fresenius Medical Care Renal Therapies Group recalls

Official ID Z-3092-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

GRANUFLO Dry Acid Concentrate recall — Fresenius Medical Care Renal Therapies Group, LLC

Complaints of blue-green discoloration in product

Company / brand: Fresenius Medical Care Renal Therapies Group recalls

Official ID Z-3091-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Brand Name recall — B Braun Medical Inc

Specific lots of Discofix Stopcock Sets recalled due to an incorrect expiration date printed on the carton shipper label.

Company / brand: B Braun Medical recalls

Official ID Z-3089-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Velys Enabling Tech Robotic-Assist Station REF recall — Medos International Sarl

Software issue within robotic controller which may cause unintended movement of the robotic arm during bone preparation or instrument positioning.

Company / brand: Medos International Sarl recalls

Official ID Z-3088-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

5008X HD/HDF with Twister Blood Tubing Set Part Number 03-5350-8 recall — Fresenius Medical Care Renal Therapies Group, LLC

Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to blood loss and hypovol…

Company / brand: Fresenius Medical Care Renal Therapies Group recalls

Official ID Z-3087-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

5008X HD/HDF with CLiC Blood Tubing Set Part number 03-5300-3C recall — Fresenius Medical Care Renal Therapies Group, LLC

Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to blood loss and hypovol…

Company / brand: Fresenius Medical Care Renal Therapies Group recalls

Official ID Z-3086-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

5008X HD/HDF Standard Blood Tubing Set Part Number 03-5300-3 recall — Fresenius Medical Care Renal Therapies Group, LLC

Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to blood loss and hypovol…

Company / brand: Fresenius Medical Care Renal Therapies Group recalls

Official ID Z-3085-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

5008X Standard HD Pre-Flush Standard Blood Tubing Set Part Number 03-5110-6 recall — Fresenius Medical Care Renal Therapies Group, LLC

Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to blood loss and hypovol…

Company / brand: Fresenius Medical Care Renal Therapies Group recalls

Official ID Z-3084-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

LUX-Dx recall — Boston Scientific Corporation

There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed notification of an AF Bu…

Company / brand: Boston Scientific recalls

Official ID Z-3083-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

LUX-Dx recall — Boston Scientific Corporation

There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed notification of an AF Bu…

Company / brand: Boston Scientific recalls

Official ID Z-3082-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

LUX-Dx recall — Boston Scientific Corporation

There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed notification of an AF Bu…

Company / brand: Boston Scientific recalls

Official ID Z-3081-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators ORTHO ASPIRATION recall — Medline Industries, LP

Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…

Company / brand: Medline Industries recalls

Official ID Z-3079-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators CATARACT PREOP K recall — Medline Industries, LP

Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…

Company / brand: Medline Industries recalls

Official ID Z-3078-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators C-SECTION PREP D recall — Medline Industries, LP

Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…

Company / brand: Medline Industries recalls

Official ID Z-3077-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators LABOR CDS CDS981 recall — Medline Industries, LP

Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…

Company / brand: Medline Industries recalls

Official ID Z-3076-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators PATIENT ADMIN KI recall — Medline Industries, LP

Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…

Company / brand: Medline Industries recalls

Official ID Z-3075-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators DELUXE PRE OP KI recall — Medline Industries, LP

Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…

Company / brand: Medline Industries recalls

Official ID Z-3074-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators ADULT BLOOD CULT recall — Medline Industries, LP

Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…

Company / brand: Medline Industries recalls

Official ID Z-3073-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD CULTURE KI recall — Medline Industries, LP

Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…

Company / brand: Medline Industries recalls

Official ID Z-3072-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators IV START KIT LAB recall — Medline Industries, LP

Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…

Company / brand: Medline Industries recalls

Official ID Z-3071-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD CULTURE PI recall — Medline Industries, LP

Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…

Company / brand: Medline Industries recalls

Official ID Z-3070-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BASIN PACK-LF DY recall — Medline Industries, LP

Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…

Company / brand: Medline Industries recalls

Official ID Z-3069-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators OPEN HEART CDS98 recall — Medline Industries, LP

Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…

Company / brand: Medline Industries recalls

Official ID Z-3068-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators PAIN PRE OP KIT recall — Medline Industries, LP

Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the app…

Company / brand: Medline Industries recalls

Official ID Z-3067-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Baxter Novum IQ Syringe Pump recall — Baxter Healthcare Corporation

A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused (VTBI) remains.

Company / brand: Baxter Healthcare recalls

Official ID Z-3066-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Baxter Novum IQ Syringe Pump recall — Baxter Healthcare Corporation

A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused (VTBI) remains.

Company / brand: Baxter Healthcare recalls

Official ID Z-3065-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

HEALON EndoCoat PRO recall — Johnson & Johnson Surgical Vision, Inc.

Surgical instructions sent for viscoelastic products used during ophthalmic viscosurgical cataract procedures including in part: If resistance is encountered during insertion, with…

Company / brand: Johnson & Johnson Surgical Vision recalls

Official ID Z-3064-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…

Company / brand: Medline Industries recalls

Official ID Z-3063-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…

Company / brand: Medline Industries recalls

Official ID Z-3062-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…

Company / brand: Medline Industries recalls

Official ID Z-3061-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…

Company / brand: Medline Industries recalls

Official ID Z-3060-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…

Company / brand: Medline Industries recalls

Official ID Z-3059-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…

Company / brand: Medline Industries recalls

Official ID Z-3058-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…

Company / brand: Medline Industries recalls

Official ID Z-3057-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…

Company / brand: Medline Industries recalls

Official ID Z-3056-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…

Company / brand: Medline Industries recalls

Official ID Z-3055-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…

Company / brand: Medline Industries recalls

Official ID Z-3054-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…

Company / brand: Medline Industries recalls

Official ID Z-3053-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…

Company / brand: Medline Industries recalls

Official ID Z-3052-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…

Company / brand: Medline Industries recalls

Official ID Z-3051-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…

Company / brand: Medline Industries recalls

Official ID Z-3050-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…

Company / brand: Medline Industries recalls

Official ID Z-3049-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding whi…

Company / brand: Medline Industries recalls

Official ID Z-3048-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

STA Staclot Protein S recall — Diagnostica Stago, Inc.

A positive drift in QC values within the reagent's stated 4-hour onboard stability period was identified

Company / brand: Diagnostica Stago recalls

Official ID Z-3047-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Halyard medical convenience kits labeled as recall — AVID Medical, Inc.

The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998…

Company / brand: AVID Medical recalls

Official ID Z-3046-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

1) NEURO recall — AVID Medical, Inc.

The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998…

Company / brand: AVID Medical recalls

Official ID Z-3045-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Halyard medical convenience kits labeled as recall — AVID Medical, Inc.

The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998…

Company / brand: AVID Medical recalls

Official ID Z-3044-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Philips Brilliance CT 64 recall — Philips North America Llc

Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the equipment.

Company / brand: Philips North America recalls

Official ID Z-3043-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Philips Ingenuity CT Product Codes recall — Philips North America Llc

Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the equipment.

Company / brand: Philips North America recalls

Official ID Z-3042-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Philips IQon Spectral CT Product Codes recall — Philips North America Llc

Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the equipment.

Company / brand: Philips North America recalls

Official ID Z-3041-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Philips Brilliance recall — Philips North America Llc

Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the equipment.

Company / brand: Philips North America recalls

Official ID Z-3040-2026 · Official record ↗

FDA Class I · Food · September 9, 2026

OLA-OLA Pounded Yam (Iyan) IYANINSTANT recall — Fayus Inc.

Undeclared milk.

Company / brand: Fayus recalls

Official ID H-1329-2026 · Official record ↗

FDA Class I · Food · September 9, 2026

Frankie's Organic Plant-Based Puffs Vegan Cheddar recall — Marina Del Rey Foods inc.

Product tested positive for undeclared milk.

Company / brand: Marina Del Rey Foods recalls

Official ID H-1328-2026 · Official record ↗

FDA Class II · Food · September 9, 2026

Bread Pudding with Vanilla Sauce - KIT NET WT 4 LB (1 recall — Ukrop's Homestyle Foods LLC

Foreign object: metal fragments

Company / brand: Ukrop's Homestyle Foods recalls

Official ID H-1327-2026 · Official record ↗

FDA Class II · Food · September 9, 2026

Bread Pudding with Vanilla Sauce NET WT 13 recall — Ukrop's Homestyle Foods LLC

Foreign object: metal fragments

Company / brand: Ukrop's Homestyle Foods recalls

Official ID H-1326-2026 · Official record ↗

FDA Class III · Food · September 9, 2026

Wonton Specialist Inc recall — Wonton Specialists

Undeclared FD&C Red No. 40

Company / brand: Wonton Specialists recalls

Official ID H-1325-2026 · Official record ↗

FDA Class III · Food · September 9, 2026

Wonton Specialist Inc recall — Wonton Specialists

Undeclared FD&C Red No. 40

Company / brand: Wonton Specialists recalls

Official ID H-1324-2026 · Official record ↗

FDA Class III · Food · September 9, 2026

Wonton Specialist Inc recall — Wonton Specialists

Undeclared FD&C Red No. 40

Company / brand: Wonton Specialists recalls

Official ID H-1323-2026 · Official record ↗

FDA Class III · Food · September 9, 2026

Wonton Specialist Inc recall — Wonton Specialists

Undeclared FD&C Red No. 40

Company / brand: Wonton Specialists recalls

Official ID H-1322-2026 · Official record ↗

FDA Class III · Food · September 9, 2026

Wonton Specialist Inc recall — Wonton Specialists

Undeclared FD&C Red No. 40

Company / brand: Wonton Specialists recalls

Official ID H-1321-2026 · Official record ↗

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FDA last checked October 22, 2026 at 12:00 PM UTC.