Browse through 2,852 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
AliExpress recalls LeymanKids children's two-piece pajama sets sold online. The recall stems from a violation of mandatory flammability standards for children's sleepwear. Consumers should stop using the pajamas immediately and pursue a full refund through AliExpress.
Hi-Tech Pharmaceuticals recalled 85,950 units of Slimaglutide weight loss supplement distributed to more than 40 states. The recall cites unapproved drug claims and misbranding. Consumers who purchased Slimaglutide should not use it and should contact Hi-Tech Pharmaceuticals for refund or replacement per the recall notice.
Prime Nutrition PhytoForm Fruits & Greens Formula recall affects 85,950 units distributed nationwide. Hi-Tech Pharmaceuticals Inc. will handle refunds or replacements. The product carries unapproved drug claims and is misbranded. Consumers who purchased this product should not consume it and should contact the company for refund or replacement information.
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 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.
Hi-Tech Pharmaceuticals recalled 85,950 units of PrimeNutrition PhytoForm Fruits & Greens Formula dietary supplement on Aug. 6, 2025. The product was manufactured by Prime Nutrition and distributed nationwide. The recall cites unapproved drug claims and misbranding. Consumers should not use the product and should contact Hi-Tech Pharmaceuticals for refund or replacement.
Glenmark Pharmaceuticals Inc., USA recalls 17,496 bottles of Carvedilol tablets sold nationwide after NNCI impurity exceeded FDA limits. The recall covers lot numbers 17241257, 17241258, and 17241279 with Exp. Date 06/2026. Consumers should stop using the product and contact Glenmark or their healthcare provider for guidance.
Glenmark Pharmaceuticals recalls 14,976 bottles of Carvedilol 25 mg distributed nationwide in the United States after FDA-identified NNCI impurity exceeds limits. The impurity prompted CGMP deviation findings. Consumers should stop taking the drug and contact Glenmark or a healthcare provider 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.
Hi-Tech Pharmaceuticals recalled Joint-RX, a 600 mcg dietary supplement sold nationwide, after regulators flagged unapproved drug claims. The recall affects 85,950 units shipped to more than 40 states. Consumers should stop using the product and contact the company for refunds or replacements.
Maquet Cardiovascular recalled 98 Vasoview Hemopro 3 EVH systems nationwide across FL, IL, MD and TX after 16 out-of-box failure complaints. No serious injuries were reported. The failures occurred during limited launch before clinical use.
Hi-Tech Pharmaceuticals recalled 85,950 units of Adderex XR Strongest Focusing Aid sold nationwide after regulators found unapproved drug claims and misbranding. The product claims to boost concentration without a prescription. Consumers who bought the product should not use it and should contact the company for a refund or replacement.
Hi-Tech Pharmaceuticals recalled 85,950 units of iFORCE Joint Help Healthy Joints & Ligaments Dietary Supplement after regulators flagged unapproved drug claims. The product was distributed to 50 states. Consumers should stop using the product and contact Hi-Tech Pharmaceuticals for refund or replacement.
Westminster Pharmaceuticals recalls 16,672 boxes of Metoprolol Tartrate 50 mg tablets nationwide after nitrosamine exceeds Acceptable Daily Intake. Manufactured by Renata PLC in Bangladesh and distributed in the US by Westminster Pharmaceuticals. Consumers should stop using the product and contact their healthcare provider for guidance.
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.
Hi-Tech Pharmaceuticals recalled 85,950 units of Fish Oil Heart and Brain Health EPA/DHA Omega-3 soft gels distributed nationwide after regulators flagged unapproved drug claims. The FDA enforcement notice identifies unapproved health claims associated with the product. Consumers who bought this product should stop using it and contact Hi-Tech Pharmaceuticals for refunds or replacements.
Hi-Tech Pharmaceuticals recalled 85,950 units of Beta Sitosterol supplement distributed nationwide from Norcross, Georgia after regulators flagged unapproved drug claims and misbranding. The product claims cardiovascular support and cholesterol benefits without FDA approval. Consumers should not consume the product and should contact Hi-Tech Pharmaceuticals for refund or replacement by letter.
Olympus Corp of the Americas recalled 103,731 ViziShot 2FLEX single-use aspiration needles worldwide after officials flagged potential undetected, deformed atraumatic tips. The recall covers the NA-U403SX-4019 model. Healthcare providers must halt use immediately and follow manufacturer instructions for recall. Manufacturers say notification was by letter.