FDA Class II · Drug · June 10, 2026
HyVee recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0572-2026 · Official record ↗
FDA recalls — page 8
2,784 recent recalls from the U.S. Food & Drug Administration in our current data (last 90 days). Showing 2,101–2,400, newest first.
FDA Class II · Drug · June 10, 2026
HyVee recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0571-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
Harris Teeter recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0570-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
FAMILY WELLNESS recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0569-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
FAMILY WELLNESS recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0568-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
DISCOUNT drug mart recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0567-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
CAREone recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0566-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
CAREone recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0565-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
MARKET BASKET ANTACID Calcium Carbonate 1000 mg recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0564-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
24/7 life BY 7-ELEVEN recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0563-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
Extra strength Antacid Calcium Carbonate 750 mg recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0562-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
Good Neighbor Pharmacy recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0561-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
Good Neighbor Pharmacy recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0560-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
HALEON CALCIUM CARBONATE TUMS ANTACID recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0559-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
HALEON CALCIUM CARBONATE TUMS ANTACID recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0558-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
KIRKLAND Signature recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0557-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
Amlodipine and Olmesartan Medoxomil Tablets recall — Ascend Laboratories, LLC
Failed Dissolution Specifications: Olmesartan Medoxomil content below specifications
Company / brand: Ascend Laboratories recalls
Official ID D-0556-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
Duloxetine DR Capsules recall — Asclemed USA Inc.
CGMP Deviations; presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the FDA acceptable intake limit.
Company / brand: Asclemed USA recalls
Official ID D-0555-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
Lidocaine HCl Injection USP recall — Spectra Medical Devices, Llc
Lack of Assurance of Sterility
Company / brand: Spectra Medical Devices recalls
Official ID D-0554-2026 · Official record ↗
FDA Class III · Drug · June 10, 2026
Lidocaine HCl Injection recall — Eugia US LLC
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
Company / brand: Eugia US recalls
Official ID D-0552-2026 · Official record ↗
FDA Class II · Medical device · June 3, 2026
Medline medical convenience kit labeled as EYE TRAY-LF recall — Medline Industries, LP
Specific Medline Kits contain Cardinal Health Monoject 1mL Luer Lock Syringes, Tuberculin Print, Sterile. Cardinal Health has recalled these syringes because the outer carton and b…
Company / brand: Medline Industries recalls
Official ID Z-2260-2026 · Official record ↗
FDA Class II · Medical device · June 3, 2026
Allura system recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of service. Issues with an H…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2259-2026 · Official record ↗
FDA Class II · Medical device · June 3, 2026
Azurion system recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of service. Issues with an H…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2258-2026 · Official record ↗
FDA Class II · Medical device · June 3, 2026
GE HealthCare ApexPro v6 recall — GE Medical Systems Information Technologies Inc
GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result…
Company / brand: GE Medical Systems Information Technologies recalls
Official ID Z-2247-2026 · Official record ↗
FDA Class II · Medical device · June 3, 2026
GE HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA recall — GE Medical Systems Information Technologies Inc
GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result…
Company / brand: GE Medical Systems Information Technologies recalls
Official ID Z-2246-2026 · Official record ↗
FDA Class II · Medical device · June 3, 2026
GE HealthCare CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA recall — GE Medical Systems Information Technologies Inc
GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result…
Company / brand: GE Medical Systems Information Technologies recalls
Official ID Z-2245-2026 · Official record ↗
FDA Class II · Medical device · June 3, 2026
GE HealthCare IOU ASSY ARK2250 CARESCAPE TELEMETRY SERVER recall — GE Medical Systems Information Technologies Inc
GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result…
Company / brand: GE Medical Systems Information Technologies recalls
Official ID Z-2244-2026 · Official record ↗
FDA Class II · Medical device · June 3, 2026
GE HealthCare APEXPRO v5 recall — GE Medical Systems Information Technologies Inc
GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result…
Company / brand: GE Medical Systems Information Technologies recalls
Official ID Z-2243-2026 · Official record ↗
FDA Class II · Medical device · June 3, 2026
GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL recall — GE Medical Systems Information Technologies Inc
GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result…
Company / brand: GE Medical Systems Information Technologies recalls
Official ID Z-2242-2026 · Official record ↗
FDA Class II · Medical device · June 3, 2026
Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation recall — Medtronic Neuromodulation
A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.
Company / brand: Medtronic Neuromodulation recalls
Official ID Z-2241-2026 · Official record ↗
FDA Class II · Medical device · June 3, 2026
Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation recall — Medtronic Neuromodulation
A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.
Company / brand: Medtronic Neuromodulation recalls
Official ID Z-2240-2026 · Official record ↗
FDA Class II · Medical device · June 3, 2026
HydroMARK Breast Biopsy Site Marker recall — Devicor Medical Products Inc
Incorrect inner package labeling. Boxes labeled 4010-02-15-T3 markers may contain individual packages labeled as T4 Markers.
Company / brand: Devicor Medical Products recalls
Official ID Z-2239-2026 · Official record ↗
FDA Class I · Medical device · June 3, 2026
Automated Impella Controller (AIC) with the below product descriptions and corresponding P recall — Abiomed, Inc.
Retrospective submission for following issues identified: 1. Alarm failures, power-path faults, electrical-short risks, and inaccurate motor-current sensing were identified in cert…
Company / brand: Abiomed recalls
Official ID Z-2238-2026 · Official record ↗
FDA Class I · Medical device · June 3, 2026
Medline kits containing Huons Co recall — Medline Industries, LP
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology t…
Company / brand: Medline Industries recalls
Official ID Z-2237-2026 · Official record ↗
FDA Class I · Medical device · June 3, 2026
Medline kits containing Huons Co recall — Medline Industries, LP
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology t…
Company / brand: Medline Industries recalls
Official ID Z-2236-2026 · Official record ↗
FDA Class I · Medical device · June 3, 2026
Medline kits containing Huons Co recall — Medline Industries, LP
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology t…
Company / brand: Medline Industries recalls
Official ID Z-2235-2026 · Official record ↗
FDA Class I · Medical device · June 3, 2026
Medline kits containing Huons Co recall — Medline Industries, LP
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology t…
Company / brand: Medline Industries recalls
Official ID Z-2234-2026 · Official record ↗
FDA Class I · Medical device · June 3, 2026
Medline kits containing Huons Co recall — Medline Industries, LP
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology t…
Company / brand: Medline Industries recalls
Official ID Z-2233-2026 · Official record ↗
FDA Class I · Medical device · June 3, 2026
Medline kits containing Huons Co recall — Medline Industries, LP
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology t…
Company / brand: Medline Industries recalls
Official ID Z-2232-2026 · Official record ↗
FDA Class I · Medical device · June 3, 2026
Medline kits containing Huons Co recall — Medline Industries, LP
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology t…
Company / brand: Medline Industries recalls
Official ID Z-2231-2026 · Official record ↗
FDA Class II · Medical device · June 3, 2026
Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers recall — O&M HALYARD INC
Nitrile Exam Glove failed to meet specifications chemical permeation performance.
Company / brand: O&M HALYARD recalls
Official ID Z-2230-2026 · Official record ↗
FDA Class I · Medical device · June 3, 2026
Automated Impella Controller (AIC) recall — Abiomed, Inc.
A retrospective review identified that there are AIC units requiring specific hardware updates to address potential safety concerns. These hardware updates have been implemented th…
Company / brand: Abiomed recalls
Official ID Z-2211-2026 · Official record ↗
FDA Class I · Medical device · June 3, 2026
RelayPro Thoracic Stent-Graft System (various sizes) Reference numbers recall — Bolton Medical Inc.
Labeling update concerning proximal clasp disconnection from the outer control tube which may prevent stent graft from being released from the delivery system.
Company / brand: Bolton Medical recalls
Official ID Z-2160-2026 · Official record ↗
FDA Class I · Food · June 3, 2026
Wawa Fruit Punch Pint (16oz) recall — Wawa Beverage Company
Undeclared Milk Allergen,
Company / brand: Wawa Beverage Company recalls
Official ID H-0858-2026 · Official record ↗
FDA Class I · Food · June 3, 2026
Wawa Diet Lemonade Pint (16oz) recall — Wawa Beverage Company
Undeclared Milk Allergen,
Company / brand: Wawa Beverage Company recalls
Official ID H-0857-2026 · Official record ↗
FDA Class I · Food · June 3, 2026
Wawa Diet Iced Tea Lemon Pint (16oz) recall — Wawa Beverage Company
Undeclared Milk Allergen,
Company / brand: Wawa Beverage Company recalls
Official ID H-0856-2026 · Official record ↗
FDA Class I · Food · June 3, 2026
Wawa Iced Tea Lemon 16 oz Pint recall — Wawa Beverage Company
Undeclared Milk Allergen,
Company / brand: Wawa Beverage Company recalls
Official ID H-0855-2026 · Official record ↗
FDA Class II · Food · June 3, 2026
Fly By Jing (branded) Creamy Sesame Noodles recall — Fly By Jing Inc.
Possible cross-contamination resulting in undeclared allergen ingredient (Peanut)
Company / brand: Fly By Jing recalls
Official ID H-0854-2026 · Official record ↗
FDA Class I · Food · June 3, 2026
giant eagle Baked Pita Chips with Parmesan recall — Legacy Bakehouse LLC
Products were made with recalled California Dairies milk powder due to Salmonella.
Company / brand: Legacy Bakehouse recalls
Official ID H-0852-2026 · Official record ↗
FDA Class I · Food · June 3, 2026
Parmesan & Herb Bagel Crisps recall — Legacy Bakehouse LLC
Products were made with recalled California Dairies milk powder due to Salmonella.
Company / brand: Legacy Bakehouse recalls
Official ID H-0851-2026 · Official record ↗
FDA Class I · Food · June 3, 2026
Butter Parsley Bagel Crisps recall — Legacy Bakehouse LLC
Products were made with recalled California Dairies milk powder due to Salmonella.
Company / brand: Legacy Bakehouse recalls
Official ID H-0850-2026 · Official record ↗
FDA Class I · Food · June 3, 2026
(BULK) SPL-BEV Banana CWT (Banana Smoothie) recall — Honeyville, Inc
Firm received and used potentially contaminated (Salmonella) ingredient to manufacture various products.
Company / brand: Honeyville recalls
Official ID H-0849-2026 · Official record ↗
FDA Class III · Drug · June 3, 2026
PRED MILD recall — AbbVie Inc.
Failed Stability Specifications
Company / brand: AbbVie recalls
Official ID D-0551-2026 · Official record ↗
FDA Class III · Drug · June 3, 2026
Nicotine Transdermal System Patch recall — AVEVA Drug Delivery Systems, Inc.
Failed Impurities/Degradation Specifications: Elevated levels of oxidative-related impurities, exceeding shelf-life specifications during stability testing of individual units.
Company / brand: AVEVA Drug Delivery Systems recalls
Official ID D-0550-2026 · Official record ↗
FDA Class II · Medical device · May 27, 2026
Integris-Allura system recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leaka…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2229-2026 · Official record ↗
FDA Class II · Medical device · May 27, 2026
Allura system recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leaka…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2228-2026 · Official record ↗
FDA Class II · Medical device · May 27, 2026
Azurion system recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leaka…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2227-2026 · Official record ↗
FDA Class II · Medical device · May 27, 2026
Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF recall — C.R. Bard Inc
Due to stain present on the surface of affected foley catheters.
Company / brand: C.R. Bard recalls
Official ID Z-2226-2026 · Official record ↗
FDA Class II · Medical device · May 27, 2026
Philips Azurion systems not configured with an optional auxiliary pan handle recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Potential safety issue with Philips Azurion systems, where longitudinal and transverse table movements may be impacted due to mechanical wear of the Float Tabletop control on the c…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2225-2026 · Official record ↗
FDA Class II · Medical device · May 27, 2026
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall — Medtronic Perfusion Systems
Certain lots of product have the potential for a sterile barrier breach.
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2222-2026 · Official record ↗
FDA Class II · Medical device · May 27, 2026
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall — Medtronic Perfusion Systems
Certain lots of product have the potential for a sterile barrier breach.
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2221-2026 · Official record ↗
FDA Class II · Medical device · May 27, 2026
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR recall — Medtronic Perfusion Systems
Certain lots of product have the potential for a sterile barrier breach.
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2220-2026 · Official record ↗
FDA Class II · Medical device · May 27, 2026
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR recall — Medtronic Perfusion Systems
Certain lots of product have the potential for a sterile barrier breach.
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2219-2026 · Official record ↗
FDA Class II · Medical device · May 27, 2026
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall — Medtronic Perfusion Systems
Certain lots of product have the potential for a sterile barrier breach.
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2218-2026 · Official record ↗
FDA Class II · Medical device · May 27, 2026
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall — Medtronic Perfusion Systems
Certain lots of product have the potential for a sterile barrier breach.
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2217-2026 · Official record ↗
FDA Class II · Medical device · May 27, 2026
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall — Medtronic Perfusion Systems
Certain lots of product have the potential for a sterile barrier breach.
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2216-2026 · Official record ↗
FDA Class II · Medical device · May 27, 2026
Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR recall — Medtronic Perfusion Systems
Certain lots of product have the potential for a sterile barrier breach.
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2215-2026 · Official record ↗
FDA Class II · Medical device · May 27, 2026
Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR recall — Medtronic Perfusion Systems
Certain lots of product have the potential for a sterile barrier breach.
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2214-2026 · Official record ↗
FDA Class II · Medical device · May 27, 2026
OneLIF Interbody Cage (REF/Description) recall — Novapproach Spine, LLC
Intervertebral body fusion system straight inserter failed to properly attach to affected cages, which may result in an inability to securely engage the implant with the inserter, …
Company / brand: Novapproach Spine recalls
Official ID Z-2213-2026 · Official record ↗
FDA Class II · Medical device · May 27, 2026
Oncology Kit w/60" (152 cm) Appx 2 recall — ICU Medical, Inc.
Oncology sets/closed system transfer devices with extension sets may leak resulting in therapy delayed if noticed and corrected during setup, but if the leak occurs during therapy …
Company / brand: ICU Medical recalls
Official ID Z-2210-2026 · Official record ↗
FDA Class II · Medical device · May 27, 2026
Tangent Endoscopy recall — TANGENT ENDOSCOPY, LLC
Affected devices exhibited fractures at the distal shaft tip without complete detachment.
Company / brand: TANGENT ENDOSCOPY recalls
Official ID Z-2209-2026 · Official record ↗
FDA Class II · Medical device · May 27, 2026
Swan-Ganz Pacing Catheter recall — Becton, Dickinson and Company
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or bl…
Company / brand: Becton recalls
Official ID Z-2204-2026 · Official record ↗
FDA Class II · Medical device · May 27, 2026
Swan-Ganz Jr Catheter recall — Becton, Dickinson and Company
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or bl…
Company / brand: Becton recalls
Official ID Z-2203-2026 · Official record ↗
FDA Class II · Medical device · May 27, 2026
Swan-Ganz Catheter recall — Becton, Dickinson and Company
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or bl…
Company / brand: Becton recalls
Official ID Z-2202-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
Stoltzfus Family Farm Sour Cream and Onion cheese curds recall — Stoltzfus Family Dairy LLC
Product may be contaminated with Salmonella.
Company / brand: Stoltzfus Family Dairy recalls
Official ID H-0848-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CLASSIC WHITE NET WT 50oz (3lbs 2oz) 1 recall — Ghirardelli Chocolate Company
Potential contamination with Salmonella.
Company / brand: Ghirardelli Chocolate Company recalls
Official ID H-0847-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
GHIRARDELLI PREMIUM HOT COCOA MIX NET WT 32oz (2lbs) 907g Ingredients recall — Ghirardelli Chocolate Company
Potential contamination with Salmonella.
Company / brand: Ghirardelli Chocolate Company recalls
Official ID H-0846-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
GHIRARDELLI SWEET GROUND POWDER CHOCOLATE & COCOA NET WT 48oz (3lbs) 1 recall — Ghirardelli Chocolate Company
Potential contamination with Salmonella.
Company / brand: Ghirardelli Chocolate Company recalls
Official ID H-0845-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
GHIRARDELLI SWEET GROUND POWDER WHITE CHOCOLATE FLAVORED NET WT 50oz (3lbs 2oz) 1 recall — Ghirardelli Chocolate Company
Potential contamination with Salmonella.
Company / brand: Ghirardelli Chocolate Company recalls
Official ID H-0844-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX VANILLA NET WT 48oz (3lbs) 1 recall — Ghirardelli Chocolate Company
Potential contamination with Salmonella.
Company / brand: Ghirardelli Chocolate Company recalls
Official ID H-0843-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE FLAVORED NET WT 50oz (3lbs 2oz) 1 recall — Ghirardelli Chocolate Company
Potential contamination with Salmonella.
Company / brand: Ghirardelli Chocolate Company recalls
Official ID H-0842-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE FLAVORED NET WT 10lbs (4 recall — Ghirardelli Chocolate Company
Potential contamination with Salmonella.
Company / brand: Ghirardelli Chocolate Company recalls
Official ID H-0841-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX WHITE MOCHA NET WT 50oz (3lbs 2oz) 1 recall — Ghirardelli Chocolate Company
Potential contamination with Salmonella.
Company / brand: Ghirardelli Chocolate Company recalls
Official ID H-0840-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX MOCHA NET WT 50oz (3lbs 2oz) 1 recall — Ghirardelli Chocolate Company
Potential contamination with Salmonella.
Company / brand: Ghirardelli Chocolate Company recalls
Official ID H-0839-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX FROZEN HOT COCOA NET WT 50oz (3lbs 2oz) 1 recall — Ghirardelli Chocolate Company
Potential contamination with Salmonella.
Company / brand: Ghirardelli Chocolate Company recalls
Official ID H-0838-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
Fisher Tex Mex Trail Mix 30 oz plastic jar UPC 070690275941 recall — JOHN B SANFILIPPO & SONS INC
potential presence of Salmonella
Company / brand: JOHN B SANFILIPPO & SONS recalls
Official ID H-0836-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
Good & Gather Mexican Street Corn Trail Mix 8 oz bag UPC 085239270240 recall — JOHN B SANFILIPPO & SONS INC
potential presence of Salmonella
Company / brand: JOHN B SANFILIPPO & SONS recalls
Official ID H-0835-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
Squirrel Brand Town & Country Mix 16 oz can UPC 07223805251 and 7 recall — JOHN B SANFILIPPO & SONS INC
potential presence of Salmonella
Company / brand: JOHN B SANFILIPPO & SONS recalls
Official ID H-0834-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
Squirrel Brand Travelers Mix 16 oz can UPC 07223899166 recall — JOHN B SANFILIPPO & SONS INC
potential presence of Salmonella
Company / brand: JOHN B SANFILIPPO & SONS recalls
Official ID H-0833-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
Southern Style Nuts Hunter Mix 30 oz plastic jar UPC 085839916302 recall — JOHN B SANFILIPPO & SONS INC
potential presence of Salmonella
Company / brand: JOHN B SANFILIPPO & SONS recalls
Official ID H-0832-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
Southern Style Nuts Gourmet Hunter Mix 23 oz plastic jar UPC 085839073319 and 36 oz plasti recall — JOHN B SANFILIPPO & SONS INC
potential presence of Salmonella
Company / brand: JOHN B SANFILIPPO & SONS recalls
Official ID H-0831-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
Pork King Good Onion & Sour Cream Seasoning recall — Pork King Good, LLC
Seasoning was made with recalled California Dairies milk powder due to Salmonella contamination.
Company / brand: Pork King Good recalls
Official ID H-0830-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
Solina 6022487 Garlic Herb Topping recall — Solina U.S. Holding
potential to be contaminated with Salmonella
Company / brand: Solina U.S. Holding recalls
Official ID H-0829-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
YT 6027393 Spicy Ranch Blend recall — Solina U.S. Holding
potential to be contaminated with Salmonella
Company / brand: Solina U.S. Holding recalls
Official ID H-0828-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
Solina 6036087 Cr¿me Fraiche Spice Seasoning recall — Solina U.S. Holding
potential to be contaminated with Salmonella
Company / brand: Solina U.S. Holding recalls
Official ID H-0827-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
Solina 6036277 Garlic Cream Sauce Seasoning recall — Solina U.S. Holding
potential to be contaminated with Salmonella
Company / brand: Solina U.S. Holding recalls
Official ID H-0826-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
Solina 6036786 Instant Country Gravy Seasoning recall — Solina U.S. Holding
potential to be contaminated with Salmonella
Company / brand: Solina U.S. Holding recalls
Official ID H-0825-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
Solina 6036554 Parmesan Breadstick Sauce Seasoning recall — Solina U.S. Holding
potential to be contaminated with Salmonella
Company / brand: Solina U.S. Holding recalls
Official ID H-0824-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
Solina 6036443 Cheddar Cheese Powder Seasoning recall — Solina U.S. Holding
potential to be contaminated with Salmonella
Company / brand: Solina U.S. Holding recalls
Official ID H-0823-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
Solina 6036195 Ranch Seasoning recall — Solina U.S. Holding
potential to be contaminated with Salmonella
Company / brand: Solina U.S. Holding recalls
Official ID H-0822-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
Solina 6035687 Bayou Blackened Ranch Seasoning recall — Solina U.S. Holding
potential to be contaminated with Salmonella
Company / brand: Solina U.S. Holding recalls
Official ID H-0821-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
Solina 6035415 Sourdough Cheese Crouton Seasoning recall — Solina U.S. Holding
potential to be contaminated with Salmonella
Company / brand: Solina U.S. Holding recalls
Official ID H-0820-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
Non Fat Dry Milk 1# recall — PS Seasoning & Spices, Inc.
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Company / brand: PS Seasoning & Spices recalls
Official ID H-0819-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
PSW21585 Save A Lot Bind 50# recall — PS Seasoning & Spices, Inc.
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Company / brand: PS Seasoning & Spices recalls
Official ID H-0818-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
Blackstone Parmesan Ranch Seasoning recall — PS Seasoning & Spices, Inc.
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Company / brand: PS Seasoning & Spices recalls
Official ID H-0817-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
1P Jalapeno Heat Unit for 300 lbs of Meat recall — PS Seasoning & Spices, Inc.
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Company / brand: PS Seasoning & Spices recalls
Official ID H-0816-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
1P Original Smokehouse Unit for 300 lbs recall — PS Seasoning & Spices, Inc.
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Company / brand: PS Seasoning & Spices recalls
Official ID H-0815-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
Ellsworth Sour Cream + Onion Seasoning recall — PS Seasoning & Spices, Inc.
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Company / brand: PS Seasoning & Spices recalls
Official ID H-0814-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
C7139D1 Natural Parmesan Cheese Flavor recall — Fontana Flavors, Inc
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Company / brand: Fontana Flavors recalls
Official ID H-0813-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
VG7274D1 Natural Cream of Mushroom Type Flavor recall — Fontana Flavors, Inc
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Company / brand: Fontana Flavors recalls
Official ID H-0812-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
C0017D Natural & Artificial White Cheddar Cheese Flavor recall — Fontana Flavors, Inc
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Company / brand: Fontana Flavors recalls
Official ID H-0811-2026 · Official record ↗
FDA Class I · Food · May 27, 2026
MA Cohen's Kippered Herring vacuum packed recall — Shining Sea Fish Co. LLC
Clostridium botulinum is an uncontrolled hazard
Company / brand: Shining Sea Fish Co recalls
Official ID H-0810-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Vitamin B-Complex recall — Llorens Pharmaceuticals International Division, Inc.
Foreign object: black particulate matter
Company / brand: Llorens Pharmaceuticals International Division recalls
Official ID H-0809-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Liposomal Sleep Spray recall — Wellnov Supplements LLC
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Company / brand: Wellnov Supplements recalls
Official ID H-0808-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Liposomal B12 Spray recall — Wellnov Supplements LLC
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Company / brand: Wellnov Supplements recalls
Official ID H-0807-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Liposomal D3+B12 Spray recall — Wellnov Supplements LLC
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Company / brand: Wellnov Supplements recalls
Official ID H-0806-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Liposomal D3-5000IU Spray Dosage recall — Wellnov Supplements LLC
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Company / brand: Wellnov Supplements recalls
Official ID H-0805-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Liposomal Prenatal+Postnatal Liquid Multivitamin Drops - Iron Free recall — Wellnov Supplements LLC
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Company / brand: Wellnov Supplements recalls
Official ID H-0804-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Liposomal Women's Liquid Multivitamin Drops - Iron Free recall — Wellnov Supplements LLC
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Company / brand: Wellnov Supplements recalls
Official ID H-0803-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Liposomal Kids Liquid Multivitamin Drops recall — Wellnov Supplements LLC
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Company / brand: Wellnov Supplements recalls
Official ID H-0802-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Liposomal Collagen Booster recall — Wellnov Supplements LLC
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Company / brand: Wellnov Supplements recalls
Official ID H-0801-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Liposomal Women's Liquid Multivitamin Drops with Iron recall — Wellnov Supplements LLC
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Company / brand: Wellnov Supplements recalls
Official ID H-0800-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Liposomal Mens 50+ Liquid Multivitamin Drops recall — Wellnov Supplements LLC
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Company / brand: Wellnov Supplements recalls
Official ID H-0799-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Liposomal Mens Liquid Multivitamin Drops recall — Wellnov Supplements LLC
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Company / brand: Wellnov Supplements recalls
Official ID H-0798-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Liposomal Womens 50+ Liquid Multivitamin Drops recall — Wellnov Supplements LLC
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Company / brand: Wellnov Supplements recalls
Official ID H-0797-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
FulviLife Complex recall — Wellnov Supplements LLC
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Company / brand: Wellnov Supplements recalls
Official ID H-0796-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Joint Nourish recall — Wellnov Supplements LLC
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen contamination and possible C. Botulinum concerns.
Company / brand: Wellnov Supplements recalls
Official ID H-0795-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Liquid Blenz Good Brain Tonic 16 oz and 32 oz recall — LIQUID BLENZ CORP
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
Company / brand: LIQUID BLENZ recalls
Official ID H-0794-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Flat Belly Bully 16 oz and 32 oz recall — LIQUID BLENZ CORP
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
Company / brand: LIQUID BLENZ recalls
Official ID H-0793-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Blood Pressure Bully 16 oz and 32 oz recall — LIQUID BLENZ CORP
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
Company / brand: LIQUID BLENZ recalls
Official ID H-0792-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Pure Shilajit Tonic 16 oz and 32 oz recall — LIQUID BLENZ CORP
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
Company / brand: LIQUID BLENZ recalls
Official ID H-0791-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Prostate Bully 16 oz and 32 oz recall — LIQUID BLENZ CORP
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
Company / brand: LIQUID BLENZ recalls
Official ID H-0790-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Fibroid Bully 16 oz and 32 oz recall — LIQUID BLENZ CORP
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
Company / brand: LIQUID BLENZ recalls
Official ID H-0789-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Menopause Bully 16 oz and 32 oz recall — LIQUID BLENZ CORP
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
Company / brand: LIQUID BLENZ recalls
Official ID H-0788-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Immunity Enhancer Elderberry 16 oz and 32 oz recall — LIQUID BLENZ CORP
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
Company / brand: LIQUID BLENZ recalls
Official ID H-0787-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Pure Libido Drink 16 oz and 32 oz recall — LIQUID BLENZ CORP
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
Company / brand: LIQUID BLENZ recalls
Official ID H-0786-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Pure Diabetes Bully 16 oz and 32 oz recall — LIQUID BLENZ CORP
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
Company / brand: LIQUID BLENZ recalls
Official ID H-0785-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Sea Moss Tonic 16 oz and 32 recall — LIQUID BLENZ CORP
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
Company / brand: LIQUID BLENZ recalls
Official ID H-0784-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Blackseed Bitters 16 oz and 32 oz recall — LIQUID BLENZ CORP
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
Company / brand: LIQUID BLENZ recalls
Official ID H-0783-2026 · Official record ↗
FDA Class II · Food · May 27, 2026
Liquid Blenz Soursop Bitters 16 oz and 32 oz recall — LIQUID BLENZ CORP
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
Company / brand: LIQUID BLENZ recalls
Official ID H-0782-2026 · Official record ↗
FDA Class I · Drug · May 27, 2026
MG217 Multi-Symptom Treatment Cream & Skin Protectant (colloidal oatmeal 2%) recall — Wisconsin Pharmacal Company
Microbial Contamination of Non-Sterile Products: confirmed presence of Staphylococcus Aureus.
Company / brand: Wisconsin Pharmacal Company recalls
Official ID D-0553-2026 · Official record ↗
FDA Class II · Drug · May 27, 2026
Vitamin B-Complex recall — Safecor Health, LLC
Presence of a Foreign Substance; black particles observed in liquid
Company / brand: Safecor Health recalls
Official ID D-0549-2026 · Official record ↗
FDA Class II · Drug · May 27, 2026
fentaNYL Citrate recall — IntegraDose Compounding Services LLC
Subpotent Drug
Company / brand: IntegraDose Compounding Services recalls
Official ID D-0548-2026 · Official record ↗
FDA Class II · Drug · May 27, 2026
cimzia (certolizumab pegol) recall — UCB Biosciences Inc.
Lack of Assurance of Sterility
Company / brand: UCB Biosciences recalls
Official ID D-0546-2026 · Official record ↗
FDA Class II · Drug · May 27, 2026
Erythromycin Tablets recall — Zydus Pharmaceuticals (USA) Inc
CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit
Company / brand: Zydus Pharmaceuticals (USA) recalls
Official ID D-0545-2026 · Official record ↗
FDA Class II · Drug · May 27, 2026
Erythromycin Tablets recall — Zydus Pharmaceuticals (USA) Inc
CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit
Company / brand: Zydus Pharmaceuticals (USA) recalls
Official ID D-0544-2026 · Official record ↗
FDA Class II · Drug · May 27, 2026
Estradiol Gel recall — ANI Pharmaceuticals, Inc.
Defective Container; packets were found to be either empty or partially full.
Company / brand: ANI Pharmaceuticals recalls
Official ID D-0543-2026 · Official record ↗
FDA Class II · Drug · May 27, 2026
Gas-X recall — Haleon US Holdings LLC
Labeling: Not Elsewhere Classified- Incomplete inactive ingredient information on the carton labeling.
Company / brand: Haleon US Holdings recalls
Official ID D-0542-2026 · Official record ↗
FDA Class II · Drug · May 27, 2026
Liraglutide Injection recall — Lupin Pharmaceuticals Inc.
Presence of particulate matter: a white thread-like structure in the cartridge
Company / brand: Lupin Pharmaceuticals recalls
Official ID D-0541-2026 · Official record ↗
FDA Class III · Drug · May 27, 2026
Busulfan Injection recall — Sagent Pharmaceuticals
Failed Impurities/Degradation Specifications
Company / brand: Sagent Pharmaceuticals recalls
Official ID D-0539-2026 · Official record ↗
FDA Class II · Drug · May 27, 2026
Atomoxetine Capsules HCL recall — Safecor Health, LLC
Labeling: Label Mix-Up: Atomoxetine HCl 25mg Capsule incorrectly labeled as Atomoxetine HCl 10mg Capsule.
Company / brand: Safecor Health recalls
Official ID D-0538-2026 · Official record ↗
FDA Class III · Drug · May 27, 2026
Primidone Tablets recall — Amerisource Health Services LLC
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
Company / brand: Amerisource Health Services recalls
Official ID D-0537-2026 · Official record ↗
FDA Class III · Drug · May 27, 2026
Primidone Tablets recall — Amerisource Health Services LLC
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
Company / brand: Amerisource Health Services recalls
Official ID D-0536-2026 · Official record ↗
FDA Class III · Drug · May 27, 2026
Primidone Tablets recall — Golden State Medical Supply Inc.
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
Company / brand: Golden State Medical Supply recalls
Official ID D-0535-2026 · Official record ↗
FDA Class III · Drug · May 27, 2026
Primidone Tablets recall — Golden State Medical Supply Inc.
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
Company / brand: Golden State Medical Supply recalls
Official ID D-0534-2026 · Official record ↗
FDA Class III · Drug · May 27, 2026
Primidone Tablets USP recall — Lannett Company Inc.
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
Company / brand: Lannett Company recalls
Official ID D-0533-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application recall — Medtronic Neuromodulation
Software issue: When programming the SynchroMed Pump with the A810 CP App in Flex Infusion Mode, the infusion steps should automatically be arranged in consecutive order, from earl…
Company / brand: Medtronic Neuromodulation recalls
Official ID Z-2201-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
LVIS Intraluminal Support Device recall — MICROVENTION INC.
Stent-assisted coiling device may due to commingling during manufacturing have dimensional nonconformance and/or incorrect device configuration. If device is oversized may lead to …
Company / brand: MICROVENTION recalls
Official ID Z-2200-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Medtronic Marinr Steerable recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2199-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Daig Livewire Steerable BDB recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2198-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Daig Livewire Steerable recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2197-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Daig Livewire Steerable recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2196-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Daig Livewire Steerable recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2195-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Daig Livewire Steerable recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2194-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Daig Livewire Steerable recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2193-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Daig Livewire Steerable recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2192-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Daig Livewire Steerable recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2191-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Daig Livewire Steerable recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2190-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Daig Livewire Steerable recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2189-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Daig Livewire Steerable recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2188-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Daig Livewire Steerable recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2187-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Daig Livewire Steerable recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2186-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
CS Uni-Directional w Auto ID recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2185-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
CS Uni-Directional w Auto ID recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2184-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
BW Webster Duo-Decapolar recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2183-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
BARD EP XT Steerable recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2182-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
BARD EP XT Decapolar Steerable recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2181-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
BARD Dynamic XT Steerable recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2180-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
BARD Dynamic XT Steerable recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2179-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
BARD Dynamic XT Deca Steerable recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2178-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
BARD Dynamic Tip Steerable recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2177-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
BARD Dynamic Tip Steerable recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2176-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
BARD Dynamic Tip Steerable recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2175-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
BARD Dynamic Deca Steerable recall — Stryker Sustainability Solutions
Incomplete seals on sterile product
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-2174-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Codman CerebroFlo EVD Catheter with Endexo Technology recall — Integra LifeSciences Corp. (NeuroSciences)
Out-of-specification endotoxin result that did not meet the acceptance criteria.
Company / brand: Integra LifeSciences (NeuroSciences) recalls
Official ID Z-2173-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Edwards EVOQUE tricuspid delivery system REF recall — Edwards Lifesciences, LLC
Labeling update to provide warning if functionality of the valve replacement delivery system is compromised.
Company / brand: Edwards Lifesciences recalls
Official ID Z-2172-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
ZYMUTEST HIA IgG recall — Aniara Diagnostica LLC
Kits from lot FD1265 had been packaged on 17 October 2024 and put on the market with an outdated flyer (8 October 2024), containing incorrect values for the positive control.
Company / brand: Aniara Diagnostica recalls
Official ID Z-2171-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Philips Azurion recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Potential for the bolts and plastic parts of the Cable Hose Carriers that hold the cable hose to the monitor ceiling suspension may loosen and/or break over time due to the forces …
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2170-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
QuickVue Dipstick Strep A Test recall — Quidel Corporation
Product has the potential for false positive results
Company / brand: Quidel recalls
Official ID Z-2169-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
3DIMENSIONS MAMMOGRAPHY SYSTEM recall — Hologic, Inc
Complaints have been received of systems developing loose, missing, or broken internal bolts over time.
Company / brand: Hologic recalls
Official ID Z-2168-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
SELENIA DIMENSIONS MAMMOGRAPHY SYSTEMS recall — Hologic, Inc
Complaints have been received of systems developing loose, missing, or broken internal bolts over time.
Company / brand: Hologic recalls
Official ID Z-2167-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code recall — Stryker Corporation
Due to nonconforming products being inadvertently distributed.
Company / brand: Stryker recalls
Official ID Z-2166-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Brand Name recall — Dexcom, Inc.
A software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing estimated glucose values (EGVs) and trend arrows. When the app…
Company / brand: Dexcom recalls
Official ID Z-2165-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Brand Name recall — Dexcom, Inc.
A software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing estimated glucose values (EGVs) and trend arrows. When the app…
Company / brand: Dexcom recalls
Official ID Z-2164-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Brand Name recall — Dexcom, Inc.
A software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing estimated glucose values (EGVs) and trend arrows. When the app…
Company / brand: Dexcom recalls
Official ID Z-2163-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Diowave Laser System recall — Technological Medical Advancements LLC
Software update is needed for laser systems, for topical infrared heating to provide temporary relief of minor muscle and joint pain, spasms, stiffness associated with minor arthri…
Company / brand: Technological Medical Advancements recalls
Official ID Z-2162-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
LUCAS 2 Model Number recall — Jolife AB
Due to a subset of chest compression systems/devices where the service performed on the systems were not appropriately documented (The documents for the service performed to justif…
Company / brand: Jolife AB recalls
Official ID Z-2161-2026 · Official record ↗
FDA Class I · Medical device · May 20, 2026
NextStep Antegrade Chronic Hemodialysis Catheter recall — ARROW INTERNATIONAL, LLC
16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and …
Company / brand: ARROW INTERNATIONAL recalls
Official ID Z-2159-2026 · Official record ↗
FDA Class I · Medical device · May 20, 2026
Cannon II Plus Hemodialysis Catheter recall — ARROW INTERNATIONAL, LLC
16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and …
Company / brand: ARROW INTERNATIONAL recalls
Official ID Z-2158-2026 · Official record ↗
FDA Class I · Medical device · May 20, 2026
Arrow-Clark VectorFlow Antegrade Chronic Hemodialysis Catheter recall — ARROW INTERNATIONAL, LLC
16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and …
Company / brand: ARROW INTERNATIONAL recalls
Official ID Z-2157-2026 · Official record ↗
FDA Class I · Medical device · May 20, 2026
Arrow Edge Hemodialysis Catheterization Product recall — ARROW INTERNATIONAL, LLC
16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and …
Company / brand: ARROW INTERNATIONAL recalls
Official ID Z-2156-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Revolution Apex Select recall — GE Medical Systems, LLC
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with …
Company / brand: GE Medical Systems recalls
Official ID Z-2155-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Revolution Apex recall — GE Medical Systems, LLC
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with …
Company / brand: GE Medical Systems recalls
Official ID Z-2154-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Revolution CT ES recall — GE Medical Systems, LLC
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with …
Company / brand: GE Medical Systems recalls
Official ID Z-2153-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Revolution Apex Plus recall — GE Medical Systems, LLC
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with …
Company / brand: GE Medical Systems recalls
Official ID Z-2152-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Revolution Apex Elite recall — GE Medical Systems, LLC
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with …
Company / brand: GE Medical Systems recalls
Official ID Z-2151-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Revolution CT recall — GE Medical Systems, LLC
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with …
Company / brand: GE Medical Systems recalls
Official ID Z-2150-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Revolution Ascend recall — GE Medical Systems, LLC
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with …
Company / brand: GE Medical Systems recalls
Official ID Z-2149-2026 · Official record ↗
FDA Class I · Medical device · May 20, 2026
Medline medical convenience kits recall — Medline Industries, LP
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Company / brand: Medline Industries recalls
Official ID Z-2148-2026 · Official record ↗
FDA Class I · Medical device · May 20, 2026
Medline medical convenience kits recall — Medline Industries, LP
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Company / brand: Medline Industries recalls
Official ID Z-2147-2026 · Official record ↗
FDA Class I · Medical device · May 20, 2026
Medline medical convenience kits recall — Medline Industries, LP
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Company / brand: Medline Industries recalls
Official ID Z-2146-2026 · Official record ↗
FDA Class I · Medical device · May 20, 2026
1 recall — Medline Industries, LP
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Company / brand: Medline Industries recalls
Official ID Z-2145-2026 · Official record ↗
FDA Class I · Medical device · May 20, 2026
1 recall — Medline Industries, LP
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Company / brand: Medline Industries recalls
Official ID Z-2144-2026 · Official record ↗
FDA Class I · Medical device · May 20, 2026
Medline medical convenience kits recall — Medline Industries, LP
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Company / brand: Medline Industries recalls
Official ID Z-2143-2026 · Official record ↗
FDA Class I · Medical device · May 20, 2026
Namic Preceptor Manifold recall — Medline Industries, LP
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Company / brand: Medline Industries recalls
Official ID Z-2142-2026 · Official record ↗
FDA Class I · Medical device · May 20, 2026
Namic Preceptor Manifold recall — Medline Industries, LP
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Company / brand: Medline Industries recalls
Official ID Z-2141-2026 · Official record ↗
FDA Class I · Medical device · May 20, 2026
Namic Angiographic Manifold recall — Medline Industries, LP
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Company / brand: Medline Industries recalls
Official ID Z-2140-2026 · Official record ↗
FDA Class I · Medical device · May 20, 2026
Namic Angiographic Manifold recall — Medline Industries, LP
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Company / brand: Medline Industries recalls
Official ID Z-2139-2026 · Official record ↗
FDA Class I · Medical device · May 20, 2026
Namic Angiographic Manifold recall — Medline Industries, LP
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Company / brand: Medline Industries recalls
Official ID Z-2138-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Brand Name recall — DJO, LLC
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Company / brand: DJO recalls
Official ID Z-2137-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Brand Name recall — DJO, LLC
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Company / brand: DJO recalls
Official ID Z-2136-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Brand Name recall — DJO, LLC
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Company / brand: DJO recalls
Official ID Z-2135-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
Brand Name recall — DJO, LLC
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Company / brand: DJO recalls
Official ID Z-2134-2026 · Official record ↗
FDA Class II · Medical device · May 20, 2026
On-X Mitral Heart Valve with Conform-X Sewing Ring recall — On-X Life Technologies, Inc.
Heart valves were released and distributed before all required testing was complete, so it cannot be confirmed that they meet all release specifications.
Company / brand: On-X Life Technologies recalls
Official ID Z-2133-2026 · Official record ↗
FDA Class I · Medical device · May 20, 2026
Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes wit recall — Windstone Medical Packaging, Inc.
Affected kits contain Medline Namic RA Syringes, which are recalled by their manufacturer due to risk of syringe rotating adapter unwinding during use, which may result in a loose …
Company / brand: Windstone Medical Packaging recalls
Official ID Z-2066-2026 · Official record ↗
FDA Class I · Medical device · May 20, 2026
Rolls of label stock used with the Omnicell i recall — Omnicell, Inc.
Potential for mislabeled syringe produced by the i.v.STATION device.
Company / brand: Omnicell recalls
Official ID Z-2047-2026 · Official record ↗
FDA Class I · Food · May 20, 2026
Pure Ground Ingredients-Organic Peppermint Leaf Powder recall — Pure Ground Ingredients, Inc.
Product has the potential to be contaminated with Salmonella.
Company / brand: Pure Ground Ingredients recalls
Official ID H-0853-2026 · Official record ↗
FDA Class I · Food · May 20, 2026
Kroger HOMESTYLE Cheese AND Garlic CROUTONS NET WT 5 OZ (141g) UPC 0 11110 81353 4 DISTRIB recall — Sugar Foods LLC
Possible Salmonella in croutons. The firm was notified by their supplier that the non-fat milk powder used to manufacture the product was recalled due to possible salmonella.
Company / brand: Sugar Foods recalls
Official ID H-0781-2026 · Official record ↗
FDA Class II · Food · May 20, 2026
recall — Ocinet, Inc.
Undeclared allergen ingredient (fish)
Company / brand: Ocinet recalls
Official ID H-0780-2026 · Official record ↗
FDA Class II · Food · May 20, 2026
Prospector Popcorn brand Belgian Chocolate Toffee flavored popcorn recall — Prospector Popcorn, LLC
Products contain undeclared soy, specifically soy lecithin.
Company / brand: Prospector Popcorn recalls
Official ID H-0779-2026 · Official record ↗
FDA Class II · Food · May 20, 2026
Swad Mango Flavored Masala Candy recall — Raja Foods and Vegetables Inc.
Contains undeclared Blue 1
Company / brand: Raja Foods and Vegetables recalls
Official ID H-0778-2026 · Official record ↗
FDA Class II · Food · May 20, 2026
Swad Orange Flavored Masala Candy recall — Raja Foods and Vegetables Inc.
Contains undeclared FD&C Yellow 6
Company / brand: Raja Foods and Vegetables recalls
Official ID H-0777-2026 · Official record ↗
FDA Class II · Food · May 20, 2026
Uncle Giuseppe's Marketplace Milk Chocolate Bridge Mix recall — WE R NUTS
Contains undeclared allergens (cashews, milk, and soy).
Company / brand: WE R NUTS recalls
Official ID H-0775-2026 · Official record ↗
FDA Class II · Food · May 20, 2026
Frederik's by meijer Vanilla Bourbon Trail Mix recall — Ferris Coffee and Nut Company, Inc.
Undeclared allergens (wheat and soy).
Company / brand: Ferris Coffee and Nut Company recalls
Official ID H-0774-2026 · Official record ↗
FDA Class II · Food · May 20, 2026
Alain MILLIAT recall — FINESALER LLC
Product may contain foreign objects, specifically glass.
Company / brand: FINESALER recalls
Official ID H-0773-2026 · Official record ↗
FDA Class II · Food · May 20, 2026
Dakota Honey Company the Honey Flight recall — Dakota Honey Company
Foreign object (stainless steel dust/flakes or shreds of plastic)
Company / brand: Dakota Honey Company recalls
Official ID H-0772-2026 · Official record ↗
FDA Class II · Food · May 20, 2026
Dakota Honey Company Spreadable Spun Honey recall — Dakota Honey Company
Foreign object (stainless steel dust/flakes or shreds of plastic)
Company / brand: Dakota Honey Company recalls
Official ID H-0771-2026 · Official record ↗
FDA Class II · Food · May 20, 2026
Dakota Honey Company Spreadable Spun Honey recall — Dakota Honey Company
Foreign object (stainless steel dust/flakes or shreds of plastic)
Company / brand: Dakota Honey Company recalls
Official ID H-0770-2026 · Official record ↗
FDA Class II · Food · May 20, 2026
Dakota Honey Company Spreadable Spun Honey recall — Dakota Honey Company
Foreign object (stainless steel dust/flakes or shreds of plastic)
Company / brand: Dakota Honey Company recalls
Official ID H-0769-2026 · Official record ↗
FDA Class II · Food · May 20, 2026
Dakota Honey Company Spreadable Spun Honey recall — Dakota Honey Company
Foreign object (stainless steel dust/flakes or shreds of plastic)
Company / brand: Dakota Honey Company recalls
Official ID H-0768-2026 · Official record ↗
FDA Class II · Drug · May 20, 2026
Ascend Laboratories recall — Ascend Laboratories, LLC
Failed Dissolution Specifications
Company / brand: Ascend Laboratories recalls
Official ID D-0547-2026 · Official record ↗
FDA Class II · Drug · May 20, 2026
Buprenorphine Hydrochloride recall — ENDO USA, Inc.
Crystallization; identified as Buprenorphine free base
Company / brand: ENDO USA recalls
Official ID D-0527-2026 · Official record ↗
FDA Class II · Drug · May 20, 2026
Oasis Tears PF recall — Oasis Medical, Inc.
Lack of Assurance of Sterility: The recall is being initiated out of an abundance of caution following FDA observations noted during a recent inspection of Excelvision.
Company / brand: Oasis Medical recalls
Official ID D-0525-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
ZENBONE recall — Orthorebirth Co Ltd
Resorbable bone void filler falls outside standard specifications.
Company / brand: Orthorebirth Co recalls
Official ID Z-2132-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
BioCera Fibers recall — Orthorebirth Co Ltd
Resorbable bone void filler falls outside standard specifications.
Company / brand: Orthorebirth Co recalls
Official ID Z-2131-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Surgical Packs recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2130-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
See complete list in RES recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2129-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Surgical Drapes recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2128-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2127-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2126-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2125-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2124-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2123-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2122-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2121-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2120-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2119-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2118-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2117-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2116-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2115-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
See RES for complete list recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2114-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2113-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2112-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2111-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2110-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
See full list in RES recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2109-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2108-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2107-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2106-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2105-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2104-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2103-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2102-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
See RES for complete list recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2101-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2100-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
See RES for complete list recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2099-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
See RES for complete list recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2098-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
See RES for full list recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2097-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2096-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2095-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2094-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
See RES for complete list recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2093-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2092-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2091-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2090-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Medline Convenience Kits recall — Medline Industries, LP
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2089-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
One Step P in vitro diagnostic test REF recall — DFI Co., Ltd.
The devices were distributed without required FDA premarket clearance or approval.
Company / brand: DFI Co recalls
Official ID Z-2088-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
One Step K in vitro diagnostic test REF recall — DFI Co., Ltd.
The devices were distributed without required FDA premarket clearance or approval.
Company / brand: DFI Co recalls
Official ID Z-2087-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Uric Acid in vitro diagnostic test REF recall — DFI Co., Ltd.
The devices were distributed without required FDA premarket clearance or approval.
Company / brand: DFI Co recalls
Official ID Z-2086-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
QUCARE Total Cholesterol in vitro diagnostic test REF recall — DFI Co., Ltd.
The devices were distributed without required FDA premarket clearance or approval.
Company / brand: DFI Co recalls
Official ID Z-2085-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
One Step pH in vitro diagnostic test REF recall — DFI Co., Ltd.
The devices were distributed without required FDA premarket clearance or approval.
Company / brand: DFI Co recalls
Official ID Z-2084-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
One Step UTI in vitro diagnostic test REF recall — DFI Co., Ltd.
The devices were distributed without required FDA premarket clearance or approval.
Company / brand: DFI Co recalls
Official ID Z-2083-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
One Step 10A in vitro diagnostic test recall — DFI Co., Ltd.
The devices were distributed without required FDA premarket clearance or approval.
Company / brand: DFI Co recalls
Official ID Z-2082-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
Biofire Spotfire Respiratory/Sore Throat Panel REF recall — BioFire Diagnostics, LLC
Respiratory/sore throat panel test may result in false negative results and control failures.
Company / brand: BioFire Diagnostics recalls
Official ID Z-2081-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
DEX Ophthalmic Tissue Forceps recall — Katalyst Surgical, LLC
Ophthalmic Tissue Forceps (DEX") are sterile, hand-held ophthalmic surgical instruments designed for grasping, manipulating, compressing, pulling, or joining eye and/or surrounding…
Company / brand: Katalyst Surgical recalls
Official ID Z-2080-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
DEX Ophthalmic Tissue Forceps recall — Katalyst Surgical, LLC
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Company / brand: Katalyst Surgical recalls
Official ID Z-2079-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
DEX Ophthalmic Tissue Forceps recall — Katalyst Surgical, LLC
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Company / brand: Katalyst Surgical recalls
Official ID Z-2078-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
DEX Ophthalmic Tissue Forceps recall — Katalyst Surgical, LLC
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Company / brand: Katalyst Surgical recalls
Official ID Z-2077-2026 · Official record ↗
FDA Class II · Medical device · May 13, 2026
DEX Ophthalmic Tissue Forceps recall — Katalyst Surgical, LLC
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Company / brand: Katalyst Surgical recalls
Official ID Z-2076-2026 · Official record ↗
Verify with the official sources:
- CPSC — consumer products ↗ (aggregated here)
- NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
- FDA — food, drugs, medical devices ↗ (aggregated here)
- USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
- Recalls.gov — the U.S. government’s all-agency portal ↗
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FDA last checked October 22, 2026 at 12:00 PM UTC.