Browse through 1,540 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Medline Industries recalled 22 sterile convenience kits on August 8, 2025, after discovering they had not been sterilized. The affected models include DYNJ0382730O and DYNJ61038B. This recall impacts states including Florida, Maryland, New Jersey, and Tennessee.
Medline Industries recalled 88 units of its Sterile Convenience Kits on August 8, 2025. The kits were labeled as sterile but did not undergo the required sterilization process. Healthcare providers and patients must stop using these kits immediately.
Schiller Ag recalled 266 units of the Argus PB-3000 on August 8, 2025. The vital sign monitoring instrument may trigger an error message during blood pressure measurements. The recall affects devices distributed nationwide in Montana, Wisconsin, and Illinois.
Deale International recalled Altafit af28 smartwatches on August 7, 2025. The recall affects models sold by HSN from March to May 2025. The smartwatch's charging pad poses a serious burn injury and fire hazard.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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 Phytoform Fruits & Greens Formula on August 6, 2025. The product contains unapproved drug claims and is misbranded. Consumers should not consume the product and seek a refund.
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.
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.