Recall database
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
Teva Pharmaceuticals USA, Inc. recalls 8,376 isotretinoin 40 mg capsules distributed to FL, OH, PR and MS after FDA enforcement report flags superpotent and subpotent lots. Patients should stop use and contact their healthcare providers for guidance.
Teva Pharmaceuticals USA, Inc. recalls 21,984 packages of Isotretinoin Capsules, USP, 30 mg. The lots are distributed to Florida, Ohio, Puerto Rico and Mississippi. The recall is active as of April 15, 2026.
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
Foreign material (small hard plastic fragments).
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 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.