Browse through 2,959 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Waldemar Link GmbH & Co. KG recalled 49 SL Connection Components sold worldwide after reports of potential detachment of the bushing from the screw shaft. A longitudinal fracture could occur, posing serious risks to patients. Patients and healthcare providers should stop using the device immediately and follow recall 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,
Waldemar Link GmbH & Co. KG recalled 4 Endo-Model Replacement Plateau devices, Item Number 15-8030/12, sold to hospitals and clinics worldwide including New Jersey. The defect involves a plateau screw, where a longitudinal fracture could cause the bushing to detach from the screw shaft. Healthcare providers and patients should stop using the device immediately and follow recall instructions from/
Waldemar Link recalled 44 Endo-Model SL implant components sold through multiple distributors worldwide, including 1 unit in the United States. The bushing could detach from the screw shaft because of a longitudinal fracture. Healthcare providers and patients should stop using the device immediately and follow recall instructions from Waldemar Link for returns or replacements.
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 implant component distributed worldwide, including New Jersey. The defect involves a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. Patients and healthcare providers should stop using the device immediately and follow the manufacturer’s recall instructions.
Waldemar Link recalled 7 Endo-Model Replacement Plateau implants worldwide, including a NJ distribution. The defect could cause the bushing to detach from the screw shaft after a longitudinal fracture. Health providers should stop use and await recall instructions.
Waldemar Link GmbH & Co. KG recalls 4 Endo-Model Replacement Plateau units worldwide, including the US state of New Jersey. A longitudinal fracture can detach the bushing from the screw shaft. Stop using the device and follow the manufacturer’s recall instructions.
Waldemar Link GmbH & Co. KG recalls 8 units of Endo-Model Replacement Plateau worldwide after a reported risk that a bushing could detach from the screw shaft due to a longitudinal fracture. The recall also covers US distribution in New Jersey. Health authorities have classified the risk as high. Patients and healthcare providers should stop using the device immediately and follow recall guidance.
McCain Foods USA recalled 67 cases of Sonic Tots on January 12, 2026, after reports of small hard plastic fragments. The frozen potato product weighs 30 lbs per case and is packaged in clear unlabeled poly bags. Consumers should not consume this product and are advised to seek a refund or replacement.
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.
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 5.4 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.
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 5,438,998 units of Sea Moss Gel on January 9, 2026. The recall follows potential contamination with Clostridium botulinum, a dangerous toxin. Consumers should not consume the product and 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 stems from potential Clostridium botulinum contamination. Consumers are urged not to 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 affected product was sold nationwide and online. Consumers should not consume the gel and should seek refunds or replacements.
Diva Fam Inc recalled 5,438,998 units of Sea Moss Gel on January 9, 2026. The product may be contaminated with Clostridium botulinum, which poses serious health risks. Consumers should stop using the product immediately and contact the company for a refund.