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Recall archive

94,355 stored notices, from Jun 20, 2012 to Sep 23, 2026.

31,892 recalls · page 50 of 1329

Consumer products

Reported May 7, 2026

Rainbow Wall Toys Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violate Mandatory Standard for…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Shenzhen Jijia Trading Co., Ltd., dba Justforjoyful

CPSC

Consumer products

Reported May 7, 2026

Svnntaa Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation Hazards; Violates…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

shenzhenkaiwendishangmaoyouxiangongsi (Shenzhen Kaiwendi Trading Co., Ltd.), dba Eokeanon

CPSC

Consumer products

Reported May 7, 2026

Multi-Purpose Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Shenzhenshilingkexunkeji Co., Ltd. (Shenzhen Lingkexun Technology Co., Ltd.), dba Foubeaka and Geniuss

CPSC

Reported May 7, 2026Updated Sep 17, 2026

Stoltzfus Family Dairy LLC recalls Stoltzfus Family Dairy Sour Cream and Onion Cheese Curds due to Potential Salmonella Contamination

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Stoltzfus Family Dairy LLC

FDA (recalls & safety alerts)

Consumer products

Reported May 7, 2026

ZMC Group Recalls Multiple Light Up Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violate…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

ZMC Group, Inc.

CPSC

Medical devices

Reported May 6, 2026

i-STAT EG7+ cartridge; List Number: 03P76-25;

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Point Of Care Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 6, 2026

Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak Model/Catalog Number: CI-5501-110;…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Advanced Bionics, LLC

FDA (openFDA device enforcement)

Reported May 6, 2026

Systane, Lubricant Eye Gel, Night Gel, Sterile, 10g (0.35 oz), Processed in France for: Alcon Laboratiroes, Inc., Fort…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alcon Research LLC

1 more product in this recall

FDA (openFDA drug enforcement)

Reported May 6, 2026

Levocarnitine Injection, USP, 1 g/5 mL (200 mg/mL), 5 mL Single-Dose Vial, For intravenous use, Rx Only, American…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

American Regent, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported May 6, 2026

BD GasPak EZ CO2 Pouch System. Catalog Number: 260684. for microbiologic use

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson & Co.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 6, 2026

iLet Bionic Pancreas, REF: BB1001

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beta Bionics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 6, 2026

Boston Scientific Pacemaker, Implantable Pulse Generator, Pacemaker (non- Cardiac Re-Synchronization Therapy) labeled…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 6, 2026

Brand Name: Kiwi Omni Vacuum Delivery System Product Name: Kiwi Omni Vacuum Delivery System Model/Catalog Number:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Clinical Innovations, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 6, 2026

Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 4 CEM. Part Number: 150450104.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Depuy (ireland)

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 6, 2026

Brand Name: Leksell Vantage Arc System REF: 1053958

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Elekta, Inc.

FDA (openFDA device enforcement)

Reported May 6, 2026

KLG, Kesar Mukhwas, perishable, 24 months, flexible plastic, 200 gm, 818812022208, Ganesha Enterprises LLC, 5200…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ganesha Enterprises LLC

FDA (openFDA food enforcement)

Reported May 6, 2026

52USA brand POPPING BOBA; STRAWBERRY FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fructose syrup, food…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Guangdong Zonegoing Food Co., Ltd.

2 more products in this recall

FDA (openFDA food enforcement)

Reported May 6, 2026

Negita Cracker- Shrimp 2.8oz

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hadson (Toko) Trading Co. Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 6, 2026

Mesh Style Tip Protectors CSW-03-2.0 Open-end style CSW-04-4.0 Closed-end style

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Healthmark Industries Co., Inc.

FDA (openFDA device enforcement)

Reported May 6, 2026

Black label with blue lettering. FOOD Korean Food, ENOKI MUSHROOM, 150g clear plastic package; Product of Korea, Keep…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Hemu Trading Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 6, 2026

Heraeus, PALAMIX uno. Material Number: 66057893.

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Heraeus Medical GmbH (Dental Division)

1 more product in this recall

FDA (openFDA device enforcement)

Reported May 6, 2026

Alendronate Sodium Oral Solution, 70 mg/75 mL, 75 mL, Rx only, 4 x 75 mL Single Dose Bottles, Distr. by: Hikma…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hikma Pharmaceuticals USA Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported May 6, 2026

Brand Name: Genius" Review Station Product Name: Genius" Review Station Display (Barco Monitor) Model/Catalog Number:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hologic, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 6, 2026

Immy, Myco DDR Trident, Bulk Neutralization Buffer B (60 X 30 mL), REF: TBPN67-60 For processing of clinical specimens…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Immuno-Mycologics, Inc.

FDA (openFDA device enforcement)

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