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.
3,615 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
McCain Foods USA Inc. recalled 21,557 cases of Ore-Ida Tater Tots on January 12, 2026, due to contamination with small hard plastic fragments. The affected product was distributed to foodservice accounts across 20 states but not sold in retail stores. Consumers should not consume the product and are advised to seek refunds or replacements.
Waldemar Link recalled 7 Endo-Model Replacement Plateau devices distributed worldwide, including New Jersey. The recall targets an implant component where a bushing could detach from the screw shaft after a longitudinal fracture. Healthcare providers and patients should stop using the device and follow recall instructions provided by the manufacturer.
Waldemar Link recalled 31 Endo-Model SL Connection Components incl. PE-Plateau sold worldwide, including New Jersey. The device bears a risk that the bushing could detach from the screw shaft due to a longitudinal fracture. Clinicians and patients should stop using the device immediately and follow manufacturer instructions.
Waldemar Link recalled 1 unit of Endo-Model Replacement Plateau worldwide, including the United States in New Jersey. The device could detach its bushing from the screw shaft because of a longitudinal fracture. Clinicians and patients should stop using the device and await manufacturer instructions.
Waldemar Link GmbH & Co. KG recalls its Endo-Model Replacement Plateau implant. Three units are affected worldwide, including New Jersey in the United States. The defect allows a bushing to detach from the screw shaft after a longitudinal fracture. Healthcare providers and patients should stop using the device immediately and follow the manufacturer’s recall instructions. Notification was sent by,
Ford Motor Company is recalling 2025 Ford Explorer and Lincoln Aviator vehicles due to a rear-view camera image that may fail when the vehicle reaches 10 mph or more. The defect could reduce rear visibility while reversing and raise crash risk. Letters to owners were mailed March 28, 2025, and Ford will provide a free APIM software update via OTA or at a dealer. Recall 24C34.
Rising Pharmaceuticals recalled 4,212 bottles of Furosemide Tablets on January 10, 2026. The recall stems from the discovery of a foreign substance in the medication. Consumers should stop using the product immediately and seek guidance from their healthcare provider.
FUJIFILM Healthcare Americas recalled 16 units of the CH-200 X-ray high-voltage generator on January 9, 2026. The electromagnetic contactors may weld, potentially causing overheating and smoke. The recall affects units distributed nationwide in various states including California and Florida.
Maquet Cardiopulmonary Gmbh recalled 3,050 Venous Bubble Sensors on January 9, 2026. Internal investigations revealed issues with the durability of the connecting cable. Excessive bending can lead to device failure, posing a risk to patient safety.
Diva Fam Inc recalled 5,438,998 units of Sea Moss Gel on January 9, 2026. The recall stems from potential Clostridium botulinum contamination. Consumers should not consume the product and seek refunds immediately.
Diva Fam Inc recalled 5,438,998 units of Sea Moss Gel on January 9, 2026, due to potential Clostridium botulinum contamination. The recall affects Soursop flavor products sold in glass jars. Consumers should stop using the product immediately and seek a refund or replacement.
Diva Fam Inc recalled approximately 5.4 million jars of Sea Moss Gel on January 9, 2026, due to potential Clostridium botulinum contamination. Consumers should not consume the product and are advised to seek refunds. The recall affects multiple lot codes sold nationwide.
Diva Fam Inc recalled 5,438,998 jars of Sea Moss Gel on January 9, 2026. The product may be contaminated with Clostridium botulinum, posing serious health risks. Consumers should not consume the product and seek refunds immediately.
Diva Fam Inc recalled approximately 5.4 million units of Sea Moss Gel on January 9, 2026. The recall stems from potential Clostridium botulinum contamination. Consumers should not consume the product and should seek refunds or replacements.
Diva Fam Inc recalled 5,438,998 jars of Sea Moss Gel on January 9, 2026. The recall stems from potential Clostridium botulinum contamination. Consumers should not consume this product and should seek refunds or replacements immediately.
Diva Fam Inc recalled approximately 5.4 million units of Sea Moss Gel on January 9, 2026. The recall stems from potential contamination with Clostridium botulinum, a dangerous toxin. Consumers should not consume this product and should seek refunds immediately.
Diva Fam Inc recalled 5.4 million jars of Sea Moss Gel on January 9, 2026. The recall follows concerns of potential Clostridium botulinum contamination. Consumers should stop using the product immediately.
Software update is needed for laser systems, for topical infrared heating to provide temporary relief of minor muscle and joint pain, spasms, stiffness associated with minor arthritis, and to temporarily increase local blood circulation, operating at a maximum average power output of 70W, which is beyond the FDA cleared 60W.
Diva Fam Inc recalled 5,438,998 jars of Sea Moss Gel on January 9, 2026 due to potential Clostridium botulinum contamination. Consumers should not consume the product and seek refunds or replacements. The recall affects various lot codes distributed nationwide.
Medartis AG recalled the 2.5 TriLock Screw 16mm HD7, 1/Pkg, sold worldwide through medical distributors including the US states of Indiana and Pennsylvania. The recall stems from a mix-up between 2.5mm and 2.8mm outer diameter screws. Healthcare providers and patients should stop using the device immediately and follow manufacturer recall instructions.