These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
2,251 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Belkin recalled portable power banks and charging stands on November 13, 2025, due to fire and burn hazards. Models MMA008, BPB002, and PB0003 are affected. Consumers should stop using these products immediately and return them for a refund.
Tesla recalled certain Powerwall 2 battery systems on November 13, 2025, due to fire and burn hazards. The recall affects units sold from November 2020 through December 2022. Consumers must stop using the units immediately to prevent serious injury or death.
Jeni's Splendid Ice Creams recalled 3,767 cases of Passion Fruit Dreamsicle Ice Cream Bars on November 13, 2025. The bars contain undeclared allergens, wheat and soy. Consumers should not consume the product and seek refunds.
Microbiologics recalled the KWIK-STIK quality control kit on November 13, 2025. The recall affects five units that may have incorrect labeling. This issue may compromise the accuracy of culture media testing for Vibrio parahaemolyticus.
American Nuts, LLC recalled 2,700 units of dry roasted macadamia nuts on November 13, 2025, due to potential Salmonella contamination. The affected product is sold in 20-ounce packages and was distributed in Hawaii. Consumers should not consume the product and seek a refund.
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.
Nissan North America recalled certain 2025 Kicks vehicles on November 12, 2025, due to a malfunctioning "Shift-to-Park" warning. The issue may lead to unexpected vehicle movement when the ignition is shut off while not in park, posing a rollaway risk. Owners will receive notification letters with further instructions, including a free fix.
Walgreens recalled 41,328 bottles of Saline Nasal Spray on November 12, 2025. The recall follows a discovery of microbial contamination by pseudomonas lactis. Consumers should stop using the product immediately and seek guidance from healthcare providers.
Cardinal Health 200 recalled 251,165 ChemoPlus gowns on November 12, 2025, due to incorrect expiration dates. The gowns are mislabeled with a five-year shelf life instead of the correct three years. Patients and healthcare providers must stop using these gowns immediately.
Genepro Protein, Inc. recalled 250 bags of Genepro Whey 4th Generation Plasma Treated Protein on November 12, 2025. The product is mislabeled and fails to declare milk as an allergen, posing a serious risk to consumers with dairy allergies. The affected product has a 'Best By' date of February 13, 2027.
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.
Stuffed Foods recalled 51 cases of Cacio e Pepe Arancini on November 12, 2025. The products contain undeclared soy protein concentrate, posing a risk to those with soy allergies. The affected items were distributed in Connecticut, Massachusetts, Florida, and Missouri.
Stryker recalled 320 units of the CranialMask Tracker on November 12, 2025, due to software errors during surgery. The device fails to activate properly, displaying an error message that prevents its use. Healthcare providers must stop using this device and follow recall instructions immediately.
AVID Medical recalled 380 units of the Halyard MINI PLUS KIT SOUTH on November 11, 2025. The devices are unsuitable for organ transplant procedures, posing potential health risks. Healthcare providers and patients must stop using the device immediately.
AVID Medical recalled 52 units of the ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17, on November 11, 2025. The devices are unsuitable for organ transplant procedures, presenting a serious health risk. Healthcare providers must stop using the device immediately and follow recall instructions.
Medline Industries recalled 163 DEXLOCK Achilles Repair Implant Kits on November 11, 2025, due to a potential hazard. Users reported drill bits fusing to the drill guide, which may prolong surgical procedures. The recall affects kits distributed nationwide in multiple states.
Dr. Reddy's Laboratories recalled 4,800 bottles of Varenicline tablets on November 11, 2025, due to sub potent drug levels. The affected lot failed stability tests, posing potential health risks to users. Consumers should stop using the product immediately and consult healthcare providers.
AVID Medical recalled 132 units of its Organ Recovery Kit on November 11, 2025. The devices are not suitable for organ transplant, posing a high risk to patients. Healthcare providers and patients should stop using the device immediately and follow recall instructions.
Kosher First recalled 283 units of Shloimy's Heimishe Matjes Herring on November 10, 2025, due to undeclared FD&C Red #40. The recall affects products distributed in New York and poses a high risk of allergic reactions. Consumers should not consume the product and seek refunds or replacements.
Draeger recalled 2,050 units of the ErgoStar CM 60 airway connector on November 10, 2025. The recall follows multiple reports of cracks in the device, posing a risk to mechanically ventilated patients. Healthcare providers and patients should stop using the connector immediately.