2,153 recalls tagged with “stop use immediately”.
TEMI Toys recalled the TEMI Go Basketball toy sold on Amazon due to a choking hazard for children under three. The toy stands about 13 inches tall and 4 inches wide and includes three yellow balls. TEMI Toys is offering a full refund to consumers who stop using the product and contact the company.
Glenmark Pharmaceuticals Inc. recalls 44,328 bottles of Carvedilol tablets, 3.125 mg, distributed nationwide in the USA. The impurity N-nitroso carvedilol I exceeds the Acceptable Intake Level. Consumers should stop using the product and contact Glenmark for guidance.
Glenmark Pharmaceuticals recalls 4,800 bottles of Carvedilol 25 mg tablets distributed nationwide in the USA. The recall cites CGMP deviations and a nitrosamine impurity exceeding the Acceptable Intake Level. Consumers should stop using the product and contact Glenmark or their healthcare provider for guidance.
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.
Hi-Tech Pharmaceuticals recalled 85,950 units of the LG Sciences Battle Hardener Platinum Series Complete 6 Week Cycle dietary supplement due to unapproved drug claims. The recall targets states across the U.S. The company is listed as Hi-Tech Pharmaceuticals. The remedy is a refund or replacement after notification by letter.
Hi-Tech Pharmaceuticals recalled 85,950 units of L-Glutamine Ultra Pure Powder distributed to multiple retailers after FDA enforcement over unapproved drug claims. The product’s labeling asserts drug-like benefits without FDA approval. Consumers should not consume the product and should contact Hi-Tech Pharmaceuticals for refund or replacement by mail to 6015-B Unity Drive, Norcross, GA 30071.
Hi-Tech Pharmaceuticals recalled 85,950 units of Formutech Nutrition Flexible Joint Formula with Cissus Quadrangularis sold nationwide after regulators flagged unapproved drug claims. The product claims to support tendons and muscles and promote healthy cartilage, which regulators say is not approved. Consumers who purchased the supplement should not use it and should await refund or replacement,'
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.
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.
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.
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.
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.
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.
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.
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.
Westminster Pharmaceuticals is recalling Metoprolol Tartrate Tablets, 100 mg, 1,000-count bottles distributed nationwide in the United States. The recall concerns CGMP deviations that led to the presence of nitrosamine N-nitroso-metoprolol above the established ADI. Consumers should stop using the product and contact Westminster for guidance.
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.
Hi-Tech Pharmaceuticals recalled 85,950 units of PrimeNutrition Taurine Mental & Athletic Performance dietary supplement distributed nationwide. The FDA enforcement report cites unapproved drug claims and misbranding. Consumers who purchased this product should not consume it and should contact the company for 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.
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.