Browse through 2,234 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
La Ligne recalled Enfant Bonne Nuit pajamas on August 7, 2025, after failing flammability standards. The 100% cotton pajamas pose a burn risk to children. Consumers should stop using them immediately and seek a refund.
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.
Petmate recalled Laser Pointer and LED Ball pet toys on August 7, 2025, due to a serious ingestion risk. The toys, sold exclusively at Menards, contain button cell batteries that can be accessed by children. Consumers should stop using them immediately and seek a full 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.
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.
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.
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.
Hi-Tech Pharmaceuticals recalled 85,950 units of its Phytoform Fruits & Greens Formula on August 6, 2025, due to unapproved drug claims. The product, sweetened with monk fruit and flavored kiwi-strawberry, poses health risks from misleading labeling. Consumers should not consume the product and seek refunds immediately.
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.
Hi-Tech Pharmaceuticals recalled 85,950 units of its fish oil soft gels on August 6, 2025, due to unapproved drug claims. The recall affects multiple states across the U.S. Consumers should stop using the product immediately.
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.
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.
Hi-Tech Pharmaceuticals recalled 85,950 units of its dietary supplement on August 6, 2025. The product contains unapproved drug claims, posing potential health risks. Consumers should stop using the supplement and seek refunds immediately.
Hi-Tech Pharmaceuticals recalled 85,950 units of its Flexible Joint Formula on August 6, 2025. The recall follows concerns over unapproved drug claims associated with the product. It was distributed across 50 states and U.S. territories.
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.
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.
Hi-Tech Pharmaceuticals recalled 85,950 units of Quercetin dietary supplements on August 6, 2025. The recall stems from unapproved drug claims and misbranding. Consumers should stop using the product and seek refunds immediately.