2,142 recalls tagged with “cpsc regulated”.
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 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.
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.
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.
Diva Fam Inc recalled 5,438,998 units of Sea Moss Gel on January 9, 2026. The product poses a risk of Clostridium botulinum contamination. Consumers should not consume the product and should seek a refund.
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 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 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.
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.
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.