poisoning risk Recalls

Wang Globalnet Recalled 1,705 Frozen Oyster Halves Over Norovirus Risk (2025)

Oyster product potentially contaminated with Norovirus

Glenmark Carvedilol 3.125 mg Recall for Nitrosamine Impurity Affects 44,328 Bottles (2025)

CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity above the current Acceptable Intake Level.

Westminster Pharmaceuticals Metoprolol Tartrate 100 mg Recalled for Nitrosamine Above ADI Level (202

CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the established Acceptable Daily Intake (ADI) level.

Hi-Tech Pharmaceuticals L-Glutamine Ultra Pure Powder Recall: 85,950 Units (2025)

Hi-Tech Pharmaceuticals Dietary Supplement LG Sciences Battle Hardener Platinum Series Recall for Un

Hi-Tech Pharmaceuticals Joint-RX Dietary Supplement Recalled for Unapproved Drug Claims (2025)

Glenmark Carvedilol 25 mg Recall Expands Over NNCI Impurity Above FDA Limit in 14,976 Bottles

CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity observed to be above the FDA-recommended limit of NMT 4.0 ppm

Glenmark Carvedilol 12.5 mg Tablets Recalled for NNCI Impurity Exceeding FDA Limit (2025)

CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity observed to be above the FDA-recommended limit of NMT 4.0 ppm

Hi-Tech Pharmaceuticals Pine Bark Supplements Recalled for Unapproved Drug Claims and Misbranding (H

Unapproved Drug Claims and Misbranded.

Hi-Tech Pharmaceuticals’ PrimeNutrition PhytoForm Fruits & Greens Recall for Unapproved Drug Claims

Unapproved Drug Claims and Misbranded.

Sandoz/Cardinal Health Enoxaparin Sodium Injection Recall Over Mispacked Bags

Enoxaparin Sodium Injection recall active as of 2025. Cardinal Health and Sandoz Inc. distributed the product in Kansas. Bags labeled 80 mg/0.8 mL contained 30 mg/0.3 mL doses. Health authorities urge immediate stop-use and guidance from providers.

M.O.M Enterprises Recalls 85,248 Organic BABY Bedtime Drops Over Spoilage Risk (2025)

Potential for spoilage due to yeast contamination.

B. Braun 23,100 0.9% Sodium Chloride Injection Containers Recalled for Sterility Concerns (2025)

B. Braun Medical Inc. recalls 23,100 0.9% Sodium Chloride Injection L 8000 containers nationwide. The recall cites lack of assurance of sterility and potential fluid leakage at a weld site. Stop using immediately and consult a healthcare provider.

Hospira Epinephrine Injection Vials Recalled for Lack of Sterility Assurance (2025)

Lack of Assurance of Sterility.

Hans Kissle Company Recalls 66 Units of Red Bliss Potato Salad for Undeclared Wheat (2025)

Contains undeclared wheat. The top label identifies the product as potato salad, but the unit contains pasta salad.

Hospira Sodium Bicarbonate Vial Recall for Sterility Concerns Affects 15,750 Vials

Lack of Assurance of Sterility.

DFA Dairy Brands Frozen Dessert Recalled for Undeclared Wheat and Soy, 324 Containers Affected

Product contains undeclared wheat and soy.

Exela Pharma Sciences 4.2% Sodium Bicarbonate Injection Recalled Over Arsenic Impurity Out-Of-Spec

Failed Impurities/Degradation Specifications: out of specification results for arsenic in the impurities tested.

Sucralfate Tablets Recall Expanded After CGMP Deviations; 26,992 Blister Packs Affected

Dynamic Sports Nutrition Recall: WINN-50 Vanazolol Dietary Supplement Sub-Potent for Vitamin B12 (H-

Dietary supplement involved degradation of an ingredient. Product is sub-potent for Vitamin B12 not meeting label claims.