Browse through 2,313 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.
AliExpress recalled LeymanKids children's pajama sets on August 7, 2025. The pajamas pose a high risk of burn injuries due to flammability violations. Consumers should stop using them immediately and contact AliExpress for a refund.
Monica Vinader recalled select 14k Yellow Gold Mini Heart Chain Bracelets, Necklaces, and Stud Earrings on August 7, 2025. The products contain high levels of cadmium, posing health risks. Consumers should stop using the items immediately and contact the company for a refund or replacement.
Fieldsheer Apparel Technologies recalled heated socks on August 7, 2025, after reports of burns. Models MWMS05, MWMS07, and MWWS07 can cause injuries during high-intensity activities. Consumers should stop using the product and seek a refund.
Guangzhou Ariel Biotech recalled Séfralls Hair Generation Serum on August 7, 2025. The recall affects an unknown number of units due to the product's non-compliance with child-resistant packaging standards. The defective packaging poses a serious poisoning risk to children if ingested.
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.
Wang Globalnet recalled 1,705 cases of frozen oysters on August 7, 2025. The product may be contaminated with Norovirus. The affected oysters were distributed across retail locations in the Northeast and Southwest regions of the U.S.
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.
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.
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.
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.
Westminster Pharmaceuticals recalled 4,456 bottles of Metoprolol Tartrate Tablets on August 6, 2025. The recall follows the detection of a nitrosamine, N-nitroso-metoprolol, above acceptable daily intake levels. Consumers should immediately stop using this medication and consult healthcare providers.
SEASPINE Orthopedics recalled 74 units of the Reef TA Inserter on August 6, 2025. The device may cause difficulties in disengaging implants, leading to prolonged surgeries. Healthcare providers should stop using the device immediately and follow recall instructions.
The Candy Barn recalled 665 packages of English Toffee on August 6, 2025. The product contains undeclared pecans, posing a risk to those with tree nut allergies. Consumers should not eat the candy and should seek a refund or replacement.
The Candy Barn recalled 665 packages of Maple Nut Fudge on August 6, 2025. The product contains undeclared allergens: pecans and eggs. Consumers should not consume the fudge and seek refunds.
The Candy Barn recalled 665 packages of its Chocolate Fudge on August 6, 2025. The product does not list egg in the allergen statement, posing a risk to those with egg allergies. Consumers should not consume the product and seek a refund.
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.
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 Pecan Toffee Clusters on August 6, 2025. The recall stems from a labeling issue where pecans were not listed in the allergen statement. Consumers should not consume these products and seek refunds.
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.