Browse through 2,317 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
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.
Draeger recalled 191,470 units of the ErgoStar CM 45 airway connector on November 10, 2025. Users reported cracks in the hose of specific catheter mounts, posing a high risk to patients. The recall affects healthcare facilities worldwide, including multiple U.S. states.
Draeger recalled 14,420 units of its ErgoStar CM 40 airway connector on November 10, 2025, due to cracks forming in the hose. The recall affects multiple states in the U.S. and several countries worldwide.
Waldemar Link GmbH & Co. KG recalled 18 units of the Endo Model Knee Fusion Nail SK on November 10, 2025. The device features a preassembled locking screw incorrectly inserted, posing a high risk of failure. Affected units were distributed in Alabama, Georgia, and Texas.
Draeger recalled 118,850 airway connectors on November 10, 2025, due to cracking hazards. This recall affects multiple countries, including the United States and Australia. The device poses a serious risk to mechanically ventilated patients.
Beckman Coulter recalled 76,098 units of COULTER DxH Diluent on November 10, 2025. The recall affects specific lots contributing to elevated platelet background counts in analyzers. Healthcare providers and patients must stop using this product immediately.