Browse through 2,852 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Glenmark Pharmaceuticals recalled 44,328 bottles of Carvedilol Tablets, USP, 3.125 mg on August 7, 2025. The recall follows the discovery of N-Nitroso Carvedilol I impurity above acceptable levels. Consumers should stop using this medication immediately and consult their healthcare providers.
Glenmark Pharmaceuticals recalled 4,800 bottles of Carvedilol Tablets on August 7, 2025. The recall stems from CGMP deviations leading to high levels of nitrosamine impurities. Consumers should stop using the product immediately and consult healthcare providers for guidance.
TEMI Toys recalled its Go Basketball children's toy on August 7, 2025. The toy poses a choking hazard due to small balls and violates safety regulations for children under three. Consumers should stop using the toy and seek a refund immediately.
Glenmark Pharmaceuticals recalled 6,432 bottles of Carvedilol Tablets on August 7, 2025. The recall stems from CGMP deviations due to the presence of a nitrosamine impurity above acceptable levels. Consumers should stop using the product immediately and contact healthcare providers for guidance.
Hi-Tech Pharmaceuticals recalled 85,950 units of its Pine Bark dietary supplement on August 6, 2025. The product contains unapproved drug claims and is misbranded. Consumers should stop using it and seek a refund.
The Candy Barn recalled 665 packages of Chocolate Mint Fudge on August 6, 2025. The product lacks proper allergen labeling for egg, posing a risk to consumers. The fudge was distributed in Kalona, Iowa at two grocery locations.
The Candy Barn recalled 665 packages of Peanut Butter Fudge on August 6, 2025. The product contains undeclared egg allergens not listed in the labeling. Consumers should not consume this fudge and seek a refund or replacement.
Hi-Tech Pharmaceuticals recalled 85,950 units of Slimaglutide on August 6, 2025. The recall is due to unapproved drug claims and misbranding. Consumers should stop using the product immediately and seek a refund or replacement.
Hi-Tech Pharmaceuticals recalled 85,950 units of its Taurine Mental & Athletic Performance dietary supplement on August 6, 2025. The company faces scrutiny for unapproved drug claims and misbranding. Consumers are urged to stop using the product immediately.
Hi-Tech Pharmaceuticals recalled 85,950 units of Adderex XR on August 6, 2025. The product faced scrutiny for unapproved drug claims and misbranding. Consumers should stop using the product immediately and seek refunds.
Hi-Tech Pharmaceuticals recalled 85,950 units of L-Glutamine Ultra Pure Powder on August 6, 2025. The recall follows concerns over unapproved drug claims associated with the product. Consumers should stop using the product and seek a refund or replacement.
iForce Nutrition recalled 85,950 units of its Joint Help dietary supplement on August 6, 2025. The recall follows concerns over unapproved drug claims. Consumers should not consume the product and seek refunds.
Glenmark Pharmaceuticals recalled 14,976 bottles of Carvedilol Tablets on August 6, 2025. The recall follows findings of N-Nitroso Carvedilol Impurity-1 above FDA limits. Consumers should stop using the product immediately and contact their healthcare provider.
Westminster Pharmaceuticals recalled 16,672 bottles of Metoprolol Tartrate Tablets on August 6, 2025. The recall stems from high levels of a harmful nitrosamine, N-nitroso-metoprolol, exceeding the Acceptable Daily Intake. Consumers must stop using the tablets immediately and consult healthcare providers for guidance.
Getinge recalled 98 units of the VASOVIEW HEMOPRO 3 Endoscopic Vessel Harvesting System on August 5, 2025. The recall addresses out-of-box failures including malfunctioning jaws and heater wires. No serious injuries were reported related to these failures.
The Candy Barn recalled 665 packages of Chocolate Pecan Fudge on August 6, 2025. The product lacks proper allergen labeling for pecans and eggs, posing a high risk to consumers. The recall affects products distributed in Kalona, Iowa.
Glenmark Pharmaceuticals recalled 17,496 bottles of Carvedilol Tablets on August 6, 2025. Tests revealed N-Nitroso Carvedilol Impurity-1 levels exceeded FDA limits. Consumers should stop using the medication immediately.
Olympus Corporation of the Americas recalled 103,731 units of the ViziShot 2FLEX aspiration needle on August 6, 2025. The recall stems from a risk of undetected, deformed a-traumatic tips that could affect patient safety. The product is distributed worldwide, including the US, Australia, and Germany.
The Candy Barn recalled 665 packages of Chocolate Walnut Fudge on August 6, 2025. The product does not list walnut and egg allergens in the 'contains' statement. Consumers should not consume the fudge and seek refunds or replacements.
The Candy Barn recalled 665 packages of Grandma's Old-Fashioned Peanut Brittle on August 6, 2025. The packaging failed to list peanuts and milk as allergens. Consumers should avoid the product and seek a refund.