1,035 recalls tagged with “chemical hazard”.
iForce Nutrition recalled 85,950 units of its Joint Help dietary supplement on August 6, 2025. The recall follows concerns over unapproved drug claims. Consumers should not consume the product and seek refunds.
Westminster Pharmaceuticals recalled 4,456 bottles of Metoprolol Tartrate Tablets on August 6, 2025. The recall follows the detection of a nitrosamine, N-nitroso-metoprolol, above acceptable daily intake levels. Consumers should immediately stop using this medication and consult healthcare providers.
Westminster Pharmaceuticals recalled 16,672 bottles of Metoprolol Tartrate Tablets on August 6, 2025. The recall stems from high levels of a harmful nitrosamine, N-nitroso-metoprolol, exceeding the Acceptable Daily Intake. Consumers must stop using the tablets immediately and consult healthcare providers for guidance.
Glenmark Pharmaceuticals recalled 14,976 bottles of Carvedilol Tablets on August 6, 2025. The recall follows findings of N-Nitroso Carvedilol Impurity-1 above FDA limits. Consumers should stop using the product immediately and contact their healthcare provider.
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.
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.
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.
Hi-Tech Pharmaceuticals recalled 85,950 units of its Taurine Mental & Athletic Performance dietary supplement on August 6, 2025. The company faces scrutiny for unapproved drug claims and misbranding. Consumers are urged to stop using the product immediately.
Hi-Tech Pharmaceuticals recalled 85,950 units of Beta Sitosterol on August 6, 2025 due to unapproved drug claims. The product supports cardiovascular health but lacks proper approval. Consumers should stop using the supplement immediately and contact the company for a refund.
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.
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 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.
Hi-Tech Pharmaceuticals recalled 85,950 units of its Phytoform Fruits & Greens Formula on August 6, 2025. The product contains unapproved drug claims and is misbranded. Consumers should stop using the product immediately and seek a refund.
Hi-Tech Pharmaceuticals recalled 85,950 units of Adderex XR on August 6, 2025. The product faced scrutiny for unapproved drug claims and misbranding. Consumers should stop using the product immediately and seek refunds.
Hi-Tech Pharmaceuticals recalled 85,950 units of its Battle Hardener dietary supplement on August 6, 2025. The product makes unapproved drug claims and poses a high health risk. Consumers should stop using the product immediately and contact the company for a refund.
Hi-Tech Pharmaceuticals recalled 85,950 units of its Joint-RX dietary supplement on August 6, 2025. The recall occurred due to unapproved drug claims related to the product. Consumers should not consume this supplement and should seek refunds or replacements.