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Recall database
All Product Recalls
Browse 4,434 active product recalls and safety alerts. Use search and filters to narrow the list by product, brand, hazard level, or status.
- Active recalls
- 4,434
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- 148
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CPSC
Belkin Recalls 3 Models of Power Banks and Charging Stands for Fire Hazard (2025)
Belkin
The lithium-ion
Health & Personal Care
HIGH
FDA DEVICE
Microbiologics KWIK-STIK QC Kit Recalled for Mislabelled Lot Packaging (2025)
Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.
Microbiologics
Some products
HIGH
CPSC
Great Lakes Wholesale International Recalled Great Lakes Select Battery Packs for Ingestion Risk (
Great Lakes Wholesale International
The button
HIGH
CPSC
Tesla Powerwall 2 Recall for Fire Hazard Affects 2020–2022 Units (2025)
This recall involves certain Tesla Powerwall 2 units, fully-integrated AC battery systems used for energy storage for self-consumption, time-based control, and backup power. Model number "Powerwall 2" is printed on the nameplate label on the side of the unit.
Tesla
The lithium-ion
MEDIUM
Food & Beverages
HIGH
FDA FOOD
American Nuts Dry Roasted Macadamia Nuts Recalled for Salmonella Contamination — 2,700 Units (2025)
American Nuts
Potential Salmonella
Food & Beverages
HIGH
FDA FOOD
MEI YU CHENG DA TRADING DRIED SALT CHILLI VEGETABLES Recalled for Banned Cyclamate Sweetener (2026)
Products contain banned sweetener: cyclamates.
MEI YU CHENG DA TRADING
Products contain
Food & Beverages
HIGH
FDA FOOD
Olive Skewers individually wrapped and packaged in clear plastic bag; 500g; INGREDIENTS: Olive, edible salt, white sugar, monosodium glutamate, licorice, cloves, food additives (citric acid, DL malic...
Products contain banned sweetener: cyclamates.
MEI YU CHENG DA TRADING
Products contain
Health & Personal Care
HIGH
FDA DRUG
Lupin Pharmaceuticals Recalls Ganirelix Acetate Injection for Impurity Risk
Lupin Pharmaceuticals recalled 32,736 vials of Ganirelix Acetate Injection on November 13, 2025. The recall follows the discovery of impurities in the drug. Consumers and healthcare providers should stop using the product immediately to avoid health risks.
GANIRELIX ACETATE
Failed impurities/degradation
Food & Beverages
HIGH
FDA FOOD
Genepro Protein Recalls 250-Bag Whey 4th Gen Plasma-Treated Protein for Milk Allergen Labeling Error
Product is mislabeled - the labeling contains incorrect ingredient information and fails to declare milk as an allergen
Genepro Protein
Product is
Vehicles & Parts
HIGH
Health & Personal Care
HIGH
FDA DRUG
Walgreens Saline Nasal Spray With Xylitol Recalled for Microbial Contamination (41,328 Bottles, 2025
Microbial contamination of a non-sterile product - microorganism found to be pseudomonas lactis
Medical Products Laboratories
Microbial contamination
Health & Personal Care
HIGH
FDA DEVICE
Cardinal Health Recalls ChemoPlus Gowns Over Expiration Date Error
Affected gowns have the incorrect expiration date on the product packaging. Product has a shelf-life of three years which is mislabeled on the product packaging as five (5) years.
Cardinal Health 200
Affected gowns
Food & Beverages
HIGH
FDA FOOD
Santos Agency Recalls Brass Langri Cookware Over Lead Risk
Santos Agency recalled Brass Langri Cookware on November 12, 2025, due to potential lead contamination. Consumers should not use the product and seek a refund. The affected item features sticker label: 14.
Santos Agency
Potential contamination
Food & Beverages
HIGH
FDA FOOD
Stuffed Foods Recalls Cacio e Pepe Arancini Over Soy Allergy Risk
Stuffed Foods
Undeclared Soy
Health & Personal Care
HIGH
FDA DEVICE
Stryker Recalls CranialMask Tracker Due to Device Error
When the device is activated during surgery, the device software issues an error message "Instrument Face Mask (6001385000000) is not valid for this application" resulting in an inability to use the device.
Howmedica Osteonics
When the
Health & Personal Care
HIGH
FDA DEVICE
Olympus Resection Sheath Recalled Due to Breakage Risk
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of the Americas
Complaints of
Health & Personal Care
HIGH
FDA DEVICE
Olympus Resection Sheath Recalled Due to Breaking Tips
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of the Americas
Complaints of