Fresh Recalls

FDA recalls — page 6

2,784 recent recalls from the U.S. Food & Drug Administration in our current data (last 90 days). Showing 1,501–1,800, newest first.

FDA Class II · Medical device · July 1, 2026

Off-Axis Comprehensive Shoulder System recall — Zimmer, Inc.

Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.

Company / brand: Zimmer recalls

Official ID Z-2528-2026 · Official record ↗

FDA Class II · Medical device · July 1, 2026

Off-Axis Comprehensive Shoulder System Small recall — Zimmer, Inc.

Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.

Company / brand: Zimmer recalls

Official ID Z-2527-2026 · Official record ↗

FDA Class II · Medical device · July 1, 2026

Multi-Snare Set recall — PFM MEDICAL INC.

A snare catheter including luer lock, indicated for removal or manipulation of a foreign body in the vascular system, failed to meet the biocompatibility requirements for in-vitro-…

Company / brand: PFM MEDICAL recalls

Official ID Z-2526-2026 · Official record ↗

FDA Class II · Medical device · July 1, 2026

VOCSN+Pro package recall — Ventec Life Systems, Inc.

Respiratory system intended to provide continuous/intermittent ventilator support, may have a damaged back-up battery supporting backup alarm function, which may result in the back…

Company / brand: Ventec Life Systems recalls

Official ID Z-2525-2026 · Official record ↗

FDA Class II · Medical device · July 1, 2026

TMJ Bilateral Implants recall — TMJ Solutions Inc

Custom temporomandibular joint implant may have contained incorrect patient-specific components that led to a poor fit of the implant, leading to a right-sided open bite.

Company / brand: TMJ Solutions recalls

Official ID Z-2524-2026 · Official record ↗

FDA Class II · Medical device · July 1, 2026

Philips Avalon Fetal Monitor recall — Philips North America Llc

Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of spe…

Company / brand: Philips North America recalls

Official ID Z-2523-2026 · Official record ↗

FDA Class II · Medical device · July 1, 2026

Philips Avalon Fetal Monitor recall — Philips North America Llc

Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of spe…

Company / brand: Philips North America recalls

Official ID Z-2522-2026 · Official record ↗

FDA Class II · Medical device · July 1, 2026

Da Vinci ASSY recall — Intuitive Surgical, Inc.

Operative components of surgical systems potentially distributed with E-brake retainer pin, so in event of a structural column failure, the E-brake pin would prevent E-brake engage…

Company / brand: Intuitive Surgical recalls

Official ID Z-2521-2026 · Official record ↗

FDA Class I · Medical device · July 1, 2026

Medline Convenience Kits recall — Medline Industries, LP

The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were rec…

Company / brand: Medline Industries recalls

Official ID Z-2455-2026 · Official record ↗

FDA Class I · Medical device · July 1, 2026

Medline Convenience Kits recall — Medline Industries, LP

The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were rec…

Company / brand: Medline Industries recalls

Official ID Z-2454-2026 · Official record ↗

FDA Class I · Medical device · July 1, 2026

Medline Convenience Kits recall — Medline Industries, LP

The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were rec…

Company / brand: Medline Industries recalls

Official ID Z-2453-2026 · Official record ↗

FDA Class I · Medical device · July 1, 2026

Medline Convenience Kits recall — Medline Industries, LP

The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were rec…

Company / brand: Medline Industries recalls

Official ID Z-2452-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

boichik bagles Pumpernickel Mix Bagels 6 pre-sliced bagels NET WT 26 recall — Boichik Bagels, Inc.

Undeclared allergen, sesame.

Company / brand: Boichik Bagels recalls

Official ID H-1133-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

boichik bagles Tuna Salad Ingredients recall — Boichik Bagels, Inc.

Ingredient statement declares eggs, but eggs are omitted from the "contains" allergen statement on the product labels.

Company / brand: Boichik Bagels recalls

Official ID H-1132-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

boichik bagels Whitefish Salad Ingredients recall — Boichik Bagels, Inc.

Ingredient statement declares eggs, but eggs are omitted from the "contains" allergen statement on the product labels.

Company / brand: Boichik Bagels recalls

Official ID H-1131-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Pearl Milling Company Original Pancake & Waffle Mix Complete (Mezcla Para Panqueques y Waf recall — CERELES EN GENERAL SAS

Undeclared allergens: Milk and Soy

Company / brand: CERELES EN GENERAL SAS recalls

Official ID H-1124-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

25# Sunflower Seeds C/S recall — George J Howe Company, Inc.

The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.

Company / brand: George J Howe Company recalls

Official ID H-1123-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

5# Sunflower Seeds C/NS recall — George J Howe Company, Inc.

The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.

Company / brand: George J Howe Company recalls

Official ID H-1122-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

5# Sunflower Seeds C/S recall — George J Howe Company, Inc.

The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.

Company / brand: George J Howe Company recalls

Official ID H-1121-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

8/9 recall — George J Howe Company, Inc.

The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.

Company / brand: George J Howe Company recalls

Official ID H-1120-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

6/11oz No Salt Sunflower Seeds recall — George J Howe Company, Inc.

The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.

Company / brand: George J Howe Company recalls

Official ID H-1119-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

6/11oz Sunflower Seeds Salted recall — George J Howe Company, Inc.

The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.

Company / brand: George J Howe Company recalls

Official ID H-1118-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

2 recall — Utz Quality Foods, LLC

Potential presence of Salmonella.

Company / brand: Utz Quality Foods recalls

Official ID H-1117-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

1 recall — Utz Quality Foods, LLC

Potential presence of Salmonella.

Company / brand: Utz Quality Foods recalls

Official ID H-1116-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

2 recall — Utz Quality Foods, LLC

Potential presence of Salmonella.

Company / brand: Utz Quality Foods recalls

Official ID H-1115-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

1 recall — Utz Quality Foods, LLC

Potential presence of Salmonella.

Company / brand: Utz Quality Foods recalls

Official ID H-1114-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

2 recall — Utz Quality Foods, LLC

Potential presence of Salmonella.

Company / brand: Utz Quality Foods recalls

Official ID H-1113-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

1 recall — Utz Quality Foods, LLC

Potential presence of Salmonella.

Company / brand: Utz Quality Foods recalls

Official ID H-1112-2026 · Official record ↗

FDA Class III · Food · July 1, 2026

Roast beef and cheddar closed face sandwich packed in clear plastic wrap with a green adhe recall — Produce Innovations

Incorrect Product Label; Roast Beef and Swiss closed face sub sandwich labeled as Turkey and Cheddar closed face sub sandwich

Company / brand: Produce Innovations recalls

Official ID H-1111-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

El David Gelee recall — Alb-USA Enterprises Inc

Undeclared colors (FD&C Yellow 5 and FD&C Red 40).

Company / brand: Alb-USA Enterprises recalls

Official ID H-1110-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Spring & Mulberry Blood Orange Date-Sweetened Chocolate recall — Spring & Mulberry Inc.

Potential Salmonella contamination

Company / brand: Spring & Mulberry recalls

Official ID H-1106-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Spring & Mulberry Coffee Date-Sweetened Chocolate recall — Spring & Mulberry Inc.

Potential Salmonella contamination

Company / brand: Spring & Mulberry recalls

Official ID H-1105-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Spring & Mulberry Sea Salt Date-Sweetened Chocolate recall — Spring & Mulberry Inc.

Potential Salmonella contamination

Company / brand: Spring & Mulberry recalls

Official ID H-1104-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

1) Spring & Mulberry Pure Dark Date-Sweetened Chocolate recall — Spring & Mulberry Inc.

Potential Salmonella contamination

Company / brand: Spring & Mulberry recalls

Official ID H-1103-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Spring & Mulberry Pecan Date Date-Sweetened Chocolate recall — Spring & Mulberry Inc.

Potential Salmonella contamination.

Company / brand: Spring & Mulberry recalls

Official ID H-1102-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Spring & Mulberry Mulberry Fennel Date-Sweetened Chocolate recall — Spring & Mulberry Inc.

Potential Salmonella contamination.

Company / brand: Spring & Mulberry recalls

Official ID H-1101-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Spring & Mulberry Mango Chili Date-Sweetened Chocolate recall — Spring & Mulberry Inc.

Potential Salmonella contamination

Company / brand: Spring & Mulberry recalls

Official ID H-1100-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Spring & Mulberry Lavender Rose Date-Sweetened Chocolate recall — Spring & Mulberry Inc.

Potential Salmonella contamination

Company / brand: Spring & Mulberry recalls

Official ID H-1099-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Spring & Mulberry Earl Grey Date-Sweetened Chocolate recall — Spring & Mulberry Inc.

Potential Salmonella contamination

Company / brand: Spring & Mulberry recalls

Official ID H-1098-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Spring & Mulberry Mixed Berry Date-Sweetened Chocolate recall — Spring & Mulberry Inc.

Potential Salmonella contamination

Company / brand: Spring & Mulberry recalls

Official ID H-1097-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Spring & Mulberry Mint Leaf Date-Sweetened Chocolate recall — Spring & Mulberry Inc.

Potential Salmonella contamination

Company / brand: Spring & Mulberry recalls

Official ID H-1096-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Motor City Pizza Co recall — Champion Foods, LLC

potential salmonella contamination

Company / brand: Champion Foods recalls

Official ID H-1095-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Saffron Cardamon Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1094-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Orange Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1093-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Peach Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1092-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Mint Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1091-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Masala Chaash Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1090-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Plain Chaash Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1089-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Mango-Pina-Orange Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1088-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Mango-Pina-Strawberry Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1087-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Strawberry Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1086-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Pineapple Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1085-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Salty Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1084-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Sweet Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1083-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Rose Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1082-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Mango Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1081-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Dried Herring Fish 7 oz recall — Prime Food Processing LLC.

Improperly eviscerated which may result in Clostridium botulinum contamination

Company / brand: Prime Food Processing recalls

Official ID H-1080-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

Perampanel CIII Tablets recall — SUN PHARMACEUTICAL INDUSTRIES INC

Labeling: Label Mix-up: 10mg Perampanel CIII tablet was found in a Perampanel CIII bottle labeled Perampanel 6 mg tablets.

Company / brand: SUN PHARMACEUTICAL INDUSTRIES recalls

Official ID D-0628-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

Povi-One recall — Elevate Oral Care

sub potency

Company / brand: Elevate Oral Care recalls

Official ID D-0627-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

Lacosamide Tablets recall — Annora Pharma Private Limited

Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of Lacosamide Tablets USP, 100mg.

Company / brand: Annora Pharma Private recalls

Official ID D-0626-2026 · Official record ↗

FDA Class I · Drug · July 1, 2026

BD ChloraPrep FREPP Clear recall — CareFusion 213, LLC

Non-Sterility: Due to presence of Aspergillus penicillioides. And Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.

Company / brand: CareFusion 213 recalls

Official ID D-0625-2026 · Official record ↗

FDA Class I · Drug · July 1, 2026

BD ChloraPrep Clear (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (I recall — CareFusion 213, LLC

Non-Sterility: Due to presence of Aspergillus penicillioides.

Company / brand: CareFusion 213 recalls

Official ID D-0624-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

BD ChloraPrep FREPP Clear recall — CareFusion 213, LLC

Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.

Company / brand: CareFusion 213 recalls

Official ID D-0623-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

BD ChloraPrep Clear recall — CareFusion 213, LLC

Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.

Company / brand: CareFusion 213 recalls

Official ID D-0622-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

PReye Vitamin See Antioxidant Preservative Free Eye Drops recall — PReye LLC

Lack of Assurance of Sterility

Company / brand: PReye recalls

Official ID D-0621-2026 · Official record ↗

FDA Class III · Drug · July 1, 2026

hydrOXYzine Hydrochloride Oral Solution recall — ANI Pharmaceuticals, Inc.

Presence of foreign substance

Company / brand: ANI Pharmaceuticals recalls

Official ID D-0619-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag recall — Central Admixture Pharmacy Services, Inc.

Incorrect product formulation: bag did not contain copper and famotidine per label.

Company / brand: Central Admixture Pharmacy Services recalls

Official ID D-0618-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

DULOXETINE D/R recall — Direct Rx

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit

Company / brand: Direct Rx recalls

Official ID D-0617-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

Sensipar (cinacalcet) Tablets recall — Amgen, Inc.

CGMP Deviations

Company / brand: Amgen recalls

Official ID D-0616-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

Corlanor (ivabradine) tablets recall — Amgen, Inc.

Presence of Foreign Substance.

Company / brand: Amgen recalls

Official ID D-0615-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

Sensipar (cinacalcet) Tablets recall — Amgen, Inc.

CGMP Deviations

Company / brand: Amgen recalls

Official ID D-0614-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

Sensipar (cinacalcet) Tablets recall — Amgen, Inc.

CGMP Deviations

Company / brand: Amgen recalls

Official ID D-0613-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

Corlanor (ivabradine) tablets recall — Amgen, Inc.

Presence of Foreign Substance.

Company / brand: Amgen recalls

Official ID D-0612-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

Fenofibrate Capsules recall — Ajanta Pharma USA Inc

CGMP Deviations

Company / brand: Ajanta Pharma USA recalls

Official ID D-0611-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

Carton Label recall — The Harvard Drug Group LLC

Subpotent Drug

Company / brand: The Harvard Drug Group recalls

Official ID D-0609-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Brand Name recall — Thoratec LLC

Due to 11 volt Backup Battery failures.

Company / brand: Thoratec recalls

Official ID Z-2520-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Brand Name recall — Thoratec LLC

Due to 11 volt Backup Battery failures.

Company / brand: Thoratec recalls

Official ID Z-2519-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Brand Name recall — Thoratec LLC

Due to 11 volt Backup Battery failures.

Company / brand: Thoratec recalls

Official ID Z-2518-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Splashwire Hydrophilic Guide Wire recall — Merit Medical Systems, Inc.

Due to unsealed portions of pouches.

Company / brand: Merit Medical Systems recalls

Official ID Z-2517-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Brand Name recall — Inspire Medical Systems Inc.

Products are labeled with incorrect Use By Date, extending beyond the validated three-year shelf life from date of manufacturer. Material degradation of a product past its Use By D…

Company / brand: Inspire Medical Systems recalls

Official ID Z-2516-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Brand Name recall — Inspire Medical Systems Inc.

Products are labeled with incorrect Use By Date, extending beyond the validated three-year shelf life from date of manufacturer. Material degradation of a product past its Use By D…

Company / brand: Inspire Medical Systems recalls

Official ID Z-2515-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code recall — BD SWITZERLAND SARL

Due to stopcock issues when using the plastic luer-lok syringe, the connection at the Port C may over thread or continue to spin rather than tightening securely. This behavior has …

Company / brand: BD SWITZERLAND SARL recalls

Official ID Z-2514-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

iLet Bionic Pancreas recall — Beta Bionics, Inc.

The reason for the recall is: it was found in version 3.3.6 of the iLet ACE Pump firmware and all previous releases that a screen unlock failure could occur when the user successfu…

Company / brand: Beta Bionics recalls

Official ID Z-2513-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Product Name recall — Staar Surgical AG

Due to a software coding issues for calculating the implant orientation diagram printout for the implantation for toric implantable collamer lenses.

Company / brand: Staar Surgical AG recalls

Official ID Z-2509-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2508-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2507-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2506-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as CLOVIS HYSTEROSCOPY recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2505-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2504-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as BASIC GYN recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2503-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2502-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2501-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2500-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2499-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2498-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as BIOBURDEN TEST KIT recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2497-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2496-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2495-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2494-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2493-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2492-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2491-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2490-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2489-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2488-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as CH OPEN HEART recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2487-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2486-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2485-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Intermittent Latex Catheter Coude Pre-Connected to Collection Bag recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2484-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Intermittent Latex Catheter Coude Pre-Connected to Collection Bag recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2483-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Urethral Catheterization Tray and Bag recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2482-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Pre-connected Urethral Catheterization Tray and Bag recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2481-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Urethral Catheterization Tray recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2480-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Urethral Catheter recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2479-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Mito Red Light recall — MITO RED LIGHT INC

The near-infrared therapy device contains a lithium-ion battery that may malfunction, causing it to catch fire or burst into flames.

Company / brand: MITO RED LIGHT recalls

Official ID Z-2478-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Giraffe OmniBed Field Replaceable Unit (FRU) recall — GE Medical Systems, LLC

GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during tr…

Company / brand: GE Medical Systems recalls

Official ID Z-2477-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Giraffe OmniBed Carestations and Giraffe OmniBed Carestation CS1 recall — GE Medical Systems, LLC

GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during tr…

Company / brand: GE Medical Systems recalls

Official ID Z-2476-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Giraffe OmniBed recall — GE Medical Systems, LLC

GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during tr…

Company / brand: GE Medical Systems recalls

Official ID Z-2475-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip recall — ConMed Corporation

Potential for overpressure alerts.

Company / brand: ConMed recalls

Official ID Z-2474-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

ConMed AirSeal 12mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall — ConMed Corporation

Potential for overpressure alerts.

Company / brand: ConMed recalls

Official ID Z-2473-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip recall — ConMed Corporation

Potential for overpressure alerts.

Company / brand: ConMed recalls

Official ID Z-2472-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall — ConMed Corporation

Potential for overpressure alerts.

Company / brand: ConMed recalls

Official ID Z-2471-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall — ConMed Corporation

Potential for overpressure alerts.

Company / brand: ConMed recalls

Official ID Z-2470-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall — ConMed Corporation

Potential for overpressure alerts.

Company / brand: ConMed recalls

Official ID Z-2469-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall — ConMed Corporation

Potential for overpressure alerts.

Company / brand: ConMed recalls

Official ID Z-2468-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall — ConMed Corporation

Potential for overpressure alerts.

Company / brand: ConMed recalls

Official ID Z-2467-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip recall — ConMed Corporation

Potential for overpressure alerts.

Company / brand: ConMed recalls

Official ID Z-2466-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

ConMed AirSeal 12 mm Access Port and Obturator with Blunt Tip recall — ConMed Corporation

Potential for overpressure alerts.

Company / brand: ConMed recalls

Official ID Z-2465-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip recall — ConMed Corporation

Potential for overpressure alerts.

Company / brand: ConMed recalls

Official ID Z-2464-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

TRI TS BASEPLATE SIZE 4 recall — Howmedica Osteonics Corp.

Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon…

Company / brand: Howmedica Osteonics recalls

Official ID Z-2462-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

TRI TS BASEPLATE SIZE 3 recall — Howmedica Osteonics Corp.

Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon…

Company / brand: Howmedica Osteonics recalls

Official ID Z-2461-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

directCHECK ACT-LR whole blood quality control recall — Accriva Diagnostics, Inc.

Assayed Whole blood control contains labeling with incorrect performance range.

Company / brand: Accriva Diagnostics recalls

Official ID Z-2460-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Ritmed Neurological Sponges recall — AMD Medicom Inc.

Neurological sponges used to moisten or absorb biological fluid during neurological surgery and may also be used to protect the brain during incision, may not consistently meet end…

Company / brand: AMD Medicom recalls

Official ID Z-2459-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Ritmed Neurological Sponges recall — AMD Medicom Inc.

Neurological sponges used to moisten or absorb biological fluid during neurological surgery and may also be used to protect the brain during incision, may not consistently meet end…

Company / brand: AMD Medicom recalls

Official ID Z-2458-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Impella CP Set with SmartAssist recall — Abiomed, Inc.

Exposure to the low purge pressure occurrence may result in persistent low purge pressure alarms and, in some cases, interruption or loss of mechanical circulatory support.

Company / brand: Abiomed recalls

Official ID Z-2457-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

TRIGEN PROXIMAL STRAIGHT HUMERAL NAIL 8/7 X 16 recall — Smith & Nephew, Inc.

Humeral nail due to a manufacturing error is missing distal holes and if implanted may lead to revision surgery but, if the missing holes are identified before implantation, an equ…

Company / brand: Smith & Nephew recalls

Official ID Z-2456-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medtronic O-arm O2 Imaging System recall — Medtronic Navigation, Inc.-Boxborough

Potential for image artifacts caused by an anomaly in the O-arm O2 Imaging System s detector panel firmware.

Company / brand: Medtronic Navigation recalls

Official ID Z-2451-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

ALYON Surgical Lighting System recall — Steris Corporation

The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.

Company / brand: Steris recalls

Official ID Z-2450-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

HarmonyAIR A-Series Surgical Lighting System recall — Steris Corporation

The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.

Company / brand: Steris recalls

Official ID Z-2449-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

HarmonyAIR A-Series Surgical Lighting System recall — Steris Corporation

There is a potential for paint delamination (chipping/peeling) on the lighting system's light heads.

Company / brand: Steris recalls

Official ID Z-2448-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2447-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2446-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2445-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2444-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2443-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2442-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2441-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2440-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2439-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2438-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Centurion convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2437-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2436-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2435-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2434-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2433-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2432-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2431-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kit recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2430-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kit recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2429-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kit recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2428-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kit recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2427-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kit recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2426-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kit recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2425-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2424-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2423-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2422-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2421-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2420-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2419-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2418-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MINOR CATH LAB PACK DYNJ84775A OR VASCULAR ANGIO PACK DYNJ47269D PORT-A-CATH DYNJ63276G recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2417-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

BLOCK TRAY DYNJRA2119A INDWELLING NERVE BLOCK DYNJRA1011A recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2416-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline CCI Nerve Block Tray DYNJRA2742 Medline CPNB DYNJRA2716 recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2415-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline EBSI Kit EBSI1534 recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries recalls

Official ID Z-2414-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Philips Allura Xper with the following Model Numbers recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended radiation exposure and…

Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls

Official ID Z-2412-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Philips MultiDiagnost Eleva with the following Model Numbers recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended radiation exposure and…

Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls

Official ID Z-2411-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2397-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2396-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2395-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2394-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2393-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2392-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2391-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2390-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2389-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2388-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2387-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2386-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2385-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2384-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2383-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2382-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2381-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2380-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2379-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2378-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2377-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2376-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2375-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2374-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2373-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2372-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2371-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2370-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2369-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2368-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2367-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2366-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2365-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2364-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

PARACENTESIS KIT recall — ARROW INTERNATIONAL, LLC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-2363-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Automated Impella Controller (AIC) recall — Abiomed, Inc.

Potential software error in the Automated Impella Controller ("AIC" ) when used in conjunction with left ventricular Impella devices.

Company / brand: Abiomed recalls

Official ID Z-2360-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Panda Freestanding Warmer recall — Datex-Ohmeda Inc

Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the intended concentration se…

Company / brand: Datex-Ohmeda recalls

Official ID Z-2359-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Giraffe Warmer with Integrated Resuscitation System (iRes) recall — Datex-Ohmeda Inc

Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the intended concentration se…

Company / brand: Datex-Ohmeda recalls

Official ID Z-2358-2026 · Official record ↗

FDA Class I · Medical device · June 24, 2026

Giraffe Stand-alone Infant Resuscitation System recall — Datex-Ohmeda Inc

Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the intended concentration se…

Company / brand: Datex-Ohmeda recalls

Official ID Z-2357-2026 · Official record ↗

FDA Class II · Food · June 24, 2026

Adndale Magnesium Glycinate Gummies 400 mg recall — Dkiru LLC

Undeclared melatonin.

Company / brand: Dkiru recalls

Official ID H-1079-2026 · Official record ↗

FDA Class II · Food · June 24, 2026

Dairy House Ingredient Systems Strawberry Dairy Powder 05#5072-50 recall — International Food Products Corporation

Potential for Salmonella

Company / brand: International Food Products recalls

Official ID H-1078-2026 · Official record ↗

FDA Class II · Food · June 24, 2026

Dairy House Ingredient Systems Vanilla Dairy Powder recall — International Food Products Corporation

Potential for Salmonella

Company / brand: International Food Products recalls

Official ID H-1077-2026 · Official record ↗

FDA Class II · Food · June 24, 2026

Legacy Tex Dressing Stabilizer Blend #7604-50 recall — International Food Products Corporation

Product tested positive for Salmonella

Company / brand: International Food Products recalls

Official ID H-1076-2026 · Official record ↗

FDA Class I · Food · June 24, 2026

azuma foods TAKO WASABI Seasoned Octopus with Wasabi PERISHABLE/KEEP FROZEN PRODUCT OF JAP recall — Azuma Foods International Inc USA

Undeclared fish.

Company / brand: Azuma Foods International USA recalls

Official ID H-1075-2026 · Official record ↗

FDA Class I · Food · June 24, 2026

White Cheddar Seasoning packed in the following sizes and configurations recall — Jonco Industries

Products were made with recalled California Dairies milk powder due to Salmonella.

Company / brand: Jonco Industries recalls

Official ID H-0953-2026 · Official record ↗

FDA Class III · Food · June 24, 2026

Salt recall — United Salt Corp

Plain salt was labeled as iodized and iodized salt was labeled as plain.

Company / brand: United Salt recalls

Official ID H-0952-2026 · Official record ↗

FDA Class II · Food · June 24, 2026

Fairhope Roasting Company Cold Brew Coffee Concentrate recall — Fairhope Roasting Company

Product requires refrigeration but the label is missing a "Keep Refrigerated" statement

Company / brand: Fairhope Roasting Company recalls

Official ID H-0951-2026 · Official record ↗

FDA Class I · Food · June 24, 2026

Al Yaman Halawa Extra Pistachio 907g (31 recall — GREENWORLD FOOD EXPRESS (USA) LLC

Product may be contaminated with Salmonella

Company / brand: GREENWORLD FOOD EXPRESS (USA) recalls

Official ID H-0950-2026 · Official record ↗

FDA Class II · Food · June 24, 2026

Great Value Hawaiian Roll 4pk recall — United States Bakery

Firm observed oily and sticky substance on direct food contact surface packaging of finished product.

Company / brand: United States Bakery recalls

Official ID H-0949-2026 · Official record ↗

FDA Class II · Food · June 24, 2026

Nutrisystem recall — Nutrisystem Inc

Undeclared Allergen (Soy)

Company / brand: Nutrisystem recalls

Official ID H-0947-2026 · Official record ↗

FDA Class II · Food · June 24, 2026

recall — MID DOLCIARIA SRL

The product contains unapproved colors chlorophyll E140 and E141.

Company / brand: MID DOLCIARIA SRL recalls

Official ID H-0946-2026 · Official record ↗

FDA Class II · Food · June 24, 2026

CANNOLI SICILIANI intended use recall — MID DOLCIARIA SRL

The product contains unapproved colors chlorophyll E140 and E141.

Company / brand: MID DOLCIARIA SRL recalls

Official ID H-0945-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Med Pride recall — Dabur India Limited

CGMP Deviations; deficiencies observed during FDA inspection

Company / brand: Dabur India recalls

Official ID D-0642-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Med Pride recall — Dabur India Limited

CGMP Deviations; deficiencies observed during FDA inspection

Company / brand: Dabur India recalls

Official ID D-0641-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Med Pride recall — Dabur India Limited

CGMP Deviations; deficiencies observed during FDA inspection

Company / brand: Dabur India recalls

Official ID D-0640-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Med Pride recall — Dabur India Limited

CGMP Deviations; deficiencies observed during FDA inspection

Company / brand: Dabur India recalls

Official ID D-0639-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Med Pride recall — Dabur India Limited

CGMP Deviations; deficiencies observed during FDA inspection

Company / brand: Dabur India recalls

Official ID D-0638-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Med Pride recall — Dabur India Limited

CGMP Deviations; deficiencies observed during FDA inspection

Company / brand: Dabur India recalls

Official ID D-0637-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Med Pride recall — Dabur India Limited

CGMP Deviations; deficiencies observed during FDA inspection

Company / brand: Dabur India recalls

Official ID D-0636-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Med Pride recall — Dabur India Limited

CGMP Deviations; deficiencies observed during FDA inspection

Company / brand: Dabur India recalls

Official ID D-0635-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Cura Hongos recall — Dabur India Limited

CGMP Deviations; deficiencies observed during FDA inspection

Company / brand: Dabur India recalls

Official ID D-0634-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Rapidol recall — Dabur India Limited

CGMP Deviations; deficiencies observed during FDA inspection

Company / brand: Dabur India recalls

Official ID D-0633-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Lil Drug Store recall — Dabur India Limited

CGMP Deviations; deficiencies observed during FDA inspection

Company / brand: Dabur India recalls

Official ID D-0632-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Circle K recall — Dabur India Limited

CGMP Deviations; deficiencies observed during FDA inspection

Company / brand: Dabur India recalls

Official ID D-0631-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Lucky Super Soft recall — Dabur India Limited

CGMP Deviations; deficiencies observed during FDA inspection

Company / brand: Dabur India recalls

Official ID D-0630-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Lucky Super Soft recall — Dabur India Limited

CGMP Deviations; deficiencies observed during FDA inspection

Company / brand: Dabur India recalls

Official ID D-0629-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Chlorthalidone Tablets recall — Inventia Healthcare Limited

Failed Dissolution Specifications

Company / brand: Inventia Healthcare recalls

Official ID D-0610-2026 · Official record ↗

FDA Class III · Drug · June 24, 2026

Focalin XR (dexmethylphenidate HCl) 5 mg recall — Sandoz Inc

Labeling: Incorrect or Missing Lot and/or Exp Date

Company / brand: Sandoz recalls

Official ID D-0608-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

safco SensiCaine-Ultra (20% Benzocaine) recall — Keystone Industries

Defective container:may contain bottles with incomplete seals

Company / brand: Keystone Industries recalls

Official ID D-0606-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

PureLife recall — Keystone Industries

Defective container:may contain bottles with incomplete seals

Company / brand: Keystone Industries recalls

Official ID D-0605-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Dental City TOPICAL ANESTHETIC GEL recall — Keystone Industries

Defective container:may contain bottles with incomplete seals

Company / brand: Keystone Industries recalls

Official ID D-0604-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Burkhart topical anesthetic gel recall — Keystone Industries

Defective container:may contain bottles with incomplete seals

Company / brand: Keystone Industries recalls

Official ID D-0603-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

DHP Topical Anesthetic Gel recall — Keystone Industries

Defective container:may contain bottles with incomplete seals

Company / brand: Keystone Industries recalls

Official ID D-0602-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Quala Dental Products recall — Keystone Industries

Defective container:may contain bottles with incomplete seals

Company / brand: Keystone Industries recalls

Official ID D-0601-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Pearson Quality Topical Anesthetic Gel (20% Benzocaine) recall — Keystone Industries

Defective container:may contain bottles with incomplete seals

Company / brand: Keystone Industries recalls

Official ID D-0600-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Buprenorphine HCl recall — Par Health USA, LLC

Crystallization; identified as Buprenorphine free base

Company / brand: Par Health USA recalls

Official ID D-0596-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Aripiprazole Tablets USP recall — Ajanta Pharma USA Inc

Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg.

Company / brand: Ajanta Pharma USA recalls

Official ID D-0594-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Vasopressin 2 Units/2 mL in 0 recall — IntegraDose Compounding Services LLC

Subpotent Drug

Company / brand: IntegraDose Compounding Services recalls

Official ID D-0593-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

VistaPharm recall — PAI Holdings LLC

Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023

Company / brand: PAI Holdings recalls

Official ID D-0592-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

VistaPharm recall — PAI Holdings LLC

Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023

Company / brand: PAI Holdings recalls

Official ID D-0591-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

VistaPharm recall — PAI Holdings LLC

Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023

Company / brand: PAI Holdings recalls

Official ID D-0590-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

VistaPharm recall — PAI Holdings LLC

Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023

Company / brand: PAI Holdings recalls

Official ID D-0589-2026 · Official record ↗

FDA Class II · Drug · June 24, 2026

Alyacen 7/7/7 recall — Glenmark Pharmaceuticals Inc., USA

Failed Impurities/Degradation Specifications: This recall is being initiated due to out-of-specification results total impurities.

Company / brand: Glenmark Pharmaceuticals recalls

Official ID D-0588-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Orca Single Use Air/Water and Suction Valves recall — Boston Scientific Corporation

Boston Scientific is initiating a medical device removal of Orca Sterile, Single Use Air/Water and Suction Valves due to a higher than anticipated occurrence of the suction button …

Company / brand: Boston Scientific recalls

Official ID Z-2413-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Halyard recall — AVID Medical, Inc.

Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

Company / brand: AVID Medical recalls

Official ID Z-2410-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Halyard recall — AVID Medical, Inc.

Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

Company / brand: AVID Medical recalls

Official ID Z-2409-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Halyard recall — AVID Medical, Inc.

Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

Company / brand: AVID Medical recalls

Official ID Z-2408-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Halyard recall — AVID Medical, Inc.

Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

Company / brand: AVID Medical recalls

Official ID Z-2407-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

MOSAIQ Oncology Information System recall — Elekta, Inc.

Software may fail to load adapted baseline shift plan during treatment delivery when a communication error occurs.

Company / brand: Elekta recalls

Official ID Z-2406-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Merlin" Patient Care System (PCS) software Merlin" PCS 3650 programmer Model 3330 software recall — Abbott Medical

Software malfunction may occur during pacing capture threshold test of pacemaker resulting in programmer not successfully communicating the command to terminate the test.

Company / brand: Abbott Medical recalls

Official ID Z-2405-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Boston Scientific Model SC-4318 recall — Boston Scientific Neuromodulation Corporation

Sterile anchors my lack sterility assurance.

Company / brand: Boston Scientific Neuromodulation recalls

Official ID Z-2404-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Boston Scientific TCN Electrodes recall — Boston Scientific Neuromodulation Corporation

Reusable electrodes may not meet expected performance levels.

Company / brand: Boston Scientific Neuromodulation recalls

Official ID Z-2403-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Boston Scientific CSK Electrodes recall — Boston Scientific Neuromodulation Corporation

Reusable electrodes may not meet expected performance levels.

Company / brand: Boston Scientific Neuromodulation recalls

Official ID Z-2402-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Bicarby Dialysate recall — Fresenius Medical Care Holdings, Inc.

There is an error in the labeling of the GTIN on the product. When scanned; however, the case labeling, lot number, and printed labeling on the product correctly identifies the pro…

Company / brand: Fresenius Medical Care Holdings recalls

Official ID Z-2401-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit recall — Inter-Med Llc

Some units of Aluminum Chloride Gel contain the package insert for Ferric Sulfate Gel. The incorrect insert misidentifies the product and contains different first aid instructions,…

Company / brand: Inter-Med recalls

Official ID Z-2400-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Hintermann Series Talar Implant recall — DT MedTech, LLC

Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.

Company / brand: DT MedTech recalls

Official ID Z-2399-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Siemens Dimension Tacrolimus Flex Reagent Cartridge (TAC) recall — Siemens Healthcare Diagnostics, Inc.

A potential positive bias in quality control (QC) and patient sample results in three lots of the Dimension Tacrolimus (TAC) Flex reagent cartridge.

Company / brand: Siemens Healthcare Diagnostics recalls

Official ID Z-2398-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Brand Name recall — The Binding Site Group, Ltd.

It was reported that plates 2 and 3 were marked as passed , although it appeared that QC had not been performed on these plates, despite samples being measured. The potential clini…

Company / brand: The Binding Site Group recalls

Official ID Z-2362-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Medartis APTUS recall — Medartis AG

The cannulation of the CCS screw is not centered.

Company / brand: Medartis AG recalls

Official ID Z-2361-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

NexxZr T Multi A3 recall — Sagemax Bioceramics, Inc.

Yttrium-stabilized zirconium oxide discs for fixed all-ceramic dental restorations may have reduced or missing dentin layer and when used clinically in the patient's mouth there is…

Company / brand: Sagemax Bioceramics recalls

Official ID Z-2356-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog Number and Product Name T50 recall — In2bones USA, LLC

Due to the Magnetic Resonance Conditional Symbol missing on the carton, inner tray, and patient label.

Company / brand: In2bones USA recalls

Official ID Z-2355-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

DigitalDiagnost C90 Flex/Value/Chest/ER recall — Philips North America Llc

System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.

Company / brand: Philips North America recalls

Official ID Z-2354-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

SD LTM 64 PLUS recall — Micromed S.p.A.

Natus has become aware of two complaints related to the SD LTM 64 PLUS where the EEG traces acquired from two or four different amplifiers used in a multiple amplifier configuratio…

Company / brand: Micromed S.p.A recalls

Official ID Z-2353-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2352-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2351-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2350-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2349-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2348-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2347-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2346-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2345-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2344-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2343-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2342-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2341-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2340-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2339-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2338-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2337-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2336-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Product Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2335-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Brand Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2334-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Brand Name recall — Avanos Medical, Inc.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Company / brand: Avanos Medical recalls

Official ID Z-2333-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Brand Name recall — HF Acquisition Co LLC

Due to incorrect incubation process being performed on product.

Company / brand: HF Acquisition Co recalls

Official ID Z-2332-2026 · Official record ↗

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