Browse through 1,551 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Elixir by Coco March recalled tinted mineral sunscreen due to CGMP deviations. The recall affects products distributed in California, Colorado, Florida, Puerto Rico, and Washington. Consumers should stop using the product immediately and seek guidance from healthcare providers.
Sugared+Bronzed recalled 2,090 tubes of Tinted Mineral Sunscreen SPF 50 on October 10, 2025. The recall stems from current Good Manufacturing Practice deviations. Consumers should stop using the product immediately and seek guidance.
CA Botana International recalled 470 tubes of Doctor D. Schwab Controlling Cream on October 10, 2025. The recall stems from CGMP deviations that pose a high hazard risk. Consumers should stop using the product and seek guidance from healthcare providers.
CA BOTANA recalled 555 tubes of Doctor D. Schwab Controlling Balm on October 10, 2025, due to CGMP deviations. The affected product contains salicylic acid and tea tree oil. Consumers should stop using the balm immediately and contact CA BOTANA International for guidance.
Doctor D. Schwab recalled 805 tubes of Shimmery Sun Lotion Sunscreen SPF 30 on October 10, 2025. The recall follows significant deviations from current good manufacturing practices (CGMP). Consumers should stop using the product immediately and contact CA BOTANA for guidance.
CA Botana International recalled 1,167 tubes of Doctor. D. Schwab Mineral Sunscreen SPF 50 on October 10, 2025. The recall stems from current good manufacturing practices (CGMP) deviations. Affected products include Lot Code D54596 with an expiration date of January 31, 2028.
CLEARSTEM recalled 4,890 bottles of YOU ARE SUNSHINE SPF 50 sunscreen on October 10, 2025. The recall follows concerns over CGMP deviations. Consumers should stop using the product immediately and contact their healthcare provider for guidance.
Doctor D. Schwab recalled 810 tubes of Clinical Weh Weh Natural Pain Relief Gel on October 10, 2025. The recall stems from CGMP deviations that could compromise product safety. The affected product was distributed in California, Colorado, Florida, Puerto Rico, and Washington.
CA Botana International, Inc. recalled 874 tubes of Ultra Umbrella Sunscreen SPF 30 on October 10, 2025. The recall stems from CGMP deviations that may affect product safety. Consumers in CA, CO, FL, PR, and WA should stop using the product immediately.
VitaTienda Co U.S.A. recalled 3,295 bottles of Elixir by Coco March Mineral Sunscreen SPF 50 on October 10, 2025. The recall stems from CGMP deviations that could affect product safety. Consumers should stop using the sunscreen immediately and contact their healthcare provider for guidance.
Gabriel Cosmetics, Inc. recalled 1,617 tubes of Mineral Sunscreen SPF 50 on October 10, 2025, due to CGMP deviations. The affected product contains 21% zinc oxide and is distributed in California, Colorado, Florida, Puerto Rico, and Washington.
Major Pharmaceuticals recalled Gabapentin Capsules, USP, 100 mg, on October 10, 2025, due to failed impurities specifications. The recall affects several lot numbers distributed nationwide. Consumers must stop using the affected capsules immediately.
Lannett Company, Inc. recalled 46,848 bottles of Niacin Extended-release Tablets on October 10, 2025. The recall follows reports of failed dissolution specifications, which could affect medication effectiveness. Consumers should stop using the product immediately and consult healthcare providers for guidance.
Major Pharmaceuticals recalled Gabapentin Capsules, USP, 100 mg on October 10, 2025, due to failed stability testing. The recall affects capsules packaged in blister packs and sold nationwide. Consumers must stop using the product immediately and seek guidance from healthcare providers.
CA Botana International recalled 1,401 tubes of Doctor D. Schwab Flawless Skin Fluid Tinted Moisturizer on October 10, 2025. The product may not meet current Good Manufacturing Practices (CGMP). Consumers should stop using it immediately and contact the company for guidance.
Dr. Bump Natural Pain Relief Gel has been recalled due to CGMP deviations. 4,890 bottles are affected, distributed in California, Colorado, Florida, Puerto Rico, and Washington. Consumers should stop using the product immediately and contact their healthcare provider for guidance.
Mylan Institutional LLC recalled 800 vials of Haloperidol Lactate Injection on October 10, 2025, due to incorrect RFID tag labels. The product may pose a risk due to potential mislabeling affecting tracking and administration. Healthcare providers should stop using the product immediately and follow up with Safecor Health for guidance.
EcoFlow Technology recalled Delta Max 2000 Power Stations due to a fire hazard. The recall affects model EFD310, identified by a black and silver design. Consumers should stop using the product immediately and seek a firmware update for repair.
Calico Brands recalled Scripto Premium Torches on October 9, 2025. The torches pose a high risk of fire and burn injuries due to safety standard violations. Consumers should stop using the product immediately and seek a refund.
YGJT recalled baby loungers on October 9, 2025, due to risks of serious injury or death. The loungers violate safety standards, posing dangers of entrapment and falls. Consumers should stop using these products immediately and seek refunds.