chemical hazard Recalls

1,035 recalls tagged with “chemical hazard”.

Health & Personal Care
HIGH
FDA DRUG

Zydus Pharmaceuticals Recalls Chlorpromazine Hydrochloride Tablets Due to Contamination

Zydus Pharmaceuticals recalled Chlorpromazine Hydrochloride Tablets on September 3, 2025. The recall affects 100-count bottles of 50 mg tablets due to excessive levels of N-Nitroso Desmethyl Chlorpromazine. Consumers should stop using the product immediately and contact health providers for guidance.

Zydus Pharmaceuticals (USA) Inc.
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Zydus Pharmaceuticals Recalls Chlorpromazine Tablets Over Hazardous Chemical

Zydus Pharmaceuticals recalled Chlorpromazine Hydrochloride tablets on September 3, 2025. The recall affects tablets manufactured in India with high levels of a hazardous chemical. Consumers must stop using the product immediately and contact their healthcare provider.

Zydus Pharmaceuticals
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Zydus Lifesciences Recalls Chlorpromazine Tablets Over Contaminant Hazard

Zydus Lifesciences recalled Chlorpromazine Hydrochloride Tablets on September 3, 2025. The recall affects tablets with NDC 16714-051-01 due to N-Nitroso Desmethyl Chlorpromazine exceeding acceptable limits. Consumers should stop using the product immediately and consult healthcare providers.

Zydus Lifesciences
CGMP Deviations:
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Food & Beverages
HIGH
FDA FOOD

Endico Mixed Vegetables Recalled Due to Listeria Contamination

Endico Potatoes Inc recalled 280 cases of mixed vegetables on September 3, 2025. The frozen product may be contaminated with Listeria monocytogenes. It was distributed in New York, New Jersey, Connecticut, Florida, Pennsylvania, Maryland, and Washington, D.C.

Endico Potatoes
Product may
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Health & Personal Care
HIGH
FDA DRUG

Zydus Lifesciences Recalls Chlorpromazine Tablets Due to Hazard

Zydus Lifesciences recalled Chlorpromazine Hydrochloride Tablets on September 3, 2025. The tablets contain N-Nitroso Desmethyl Chlorpromazine above safe intake levels. Consumers must stop using the product immediately and consult healthcare providers.

Zydus Lifesciences
CGMP Deviations:
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Food & Beverages
HIGH
FDA FOOD

Endico Frozen Peas and Carrots Recalled Due to Listeria Risk

Endico Potatoes Inc recalled 335 cases of frozen peas and carrots on September 3, 2025. The products may contain Listeria monocytogenes, a bacteria that can cause serious illness. The affected items were distributed in several states including New York and Florida.

Endico Potatoes
Product may
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Health & Personal Care
HIGH
FDA DRUG

Zydus Recalls Chlorpromazine Hydrochloride Tablets Over Contamination Hazard

Zydus Lifesciences Ltd. recalled Chlorpromazine Hydrochloride Tablets on September 3, 2025. The recall affects 10 mg tablets sold nationwide due to contamination with N-Nitroso Desmethyl Chlorpromazine. Consumers should stop using the product immediately and consult healthcare providers.

Zydus Lifesciences
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Zydus Lifesciences Recalls Chlorpromazine Tablets Due to Contamination

Zydus Lifesciences Ltd. recalled Chlorpromazine Hydrochloride Tablets on September 3, 2025. The recall affects tablets containing N-Nitroso Desmethyl Chlorpromazine above safe limits. Consumers should stop using the product immediately and consult healthcare providers.

Zydus Lifesciences
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Zydus Lifesciences Recalls Chlorpromazine Tablets Over Chemical Hazard

Zydus Lifesciences Ltd. recalled Chlorpromazine Hydrochloride Tablets on September 3, 2025. The recall affects products with NDC 16714-050-01 due to high levels of a chemical impurity. Consumers should stop using the tablets immediately and contact healthcare providers.

Zydus Lifesciences
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter Reagents Recalled Due to Calibration Failure

Beckman Coulter recalled 2,146 units of SYNCHRON Systems Phosphorus reagents on September 3, 2025. The affected lots may fail calibration before expiration, delaying patient results. Healthcare providers must stop using the product immediately.

Beckman Coulter
Specific SYNCHRON
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Food & Beverages
HIGH
FDA FOOD

New Spirit Naturals Recalls Muscle Support Powder Due to Milk Allergen

New Spirit Naturals recalled 178 units of Super Muscle Support Powder on September 3, 2025. The product contains an undeclared allergen, milk, posing a serious health risk. Consumers should stop using the product immediately and contact the company for a refund.

New Spirit Naturals
undeclared allergen
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Food & Beverages
HIGH
FDA FOOD

New Spirit Naturals Recalls Protein Powder Over Milk Allergen Risk

New Spirit Naturals recalled 79 units of Meal In A Glass protein powder on September 3, 2025. The recall affects 1.05 lbs and 4.5 lbs containers of Vanilla, Chocolate, and Strawberry flavors. The product contains undeclared milk, posing a serious risk to consumers with milk allergies.

New Spirit Naturals
undeclared allergen
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Health & Personal Care
HIGH
FDA DRUG

Glenmark Pharmaceuticals Recalls Viorele Tablets Over Impurity Issues

Glenmark Pharmaceuticals recalled 26,928 packs of Viorele oral contraceptives on September 3, 2025. The recall follows the discovery of impurity issues in the product. Consumers should stop using the affected tablets immediately and contact healthcare providers for guidance.

Viorele
Failed Impurities/Degradation
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Food & Beverages
HIGH
FDA FOOD

New Spirit Naturals Recalls Gluta Plus Capsules Over Milk Allergen

New Spirit Naturals recalled 83 units of Gluta Plus (Glutathione) on September 3, 2025, due to undeclared milk allergens. The recall affects specific lot codes and poses a high risk to consumers with milk allergies. This recall is active, and consumers should stop using the product immediately.

New Spirit Naturals
undeclared allergen
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Health & Personal Care
HIGH
FDA DRUG

Cardinal Health Recalls Sulfamethoxazole and Trimethoprim Over Microbial Risk

Cardinal Health recalled Sulfamethoxazole and Trimethoprim tablets on September 2, 2025, due to contamination risks. A specific lot contained a foreign substance with a detected micro-organism, although no contamination was found on the tablets. Consumers must stop using the product immediately and seek guidance from healthcare providers.

SULFAMETHOXAZOLE AND TRIMETHOPRIM
Presence of
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Health & Personal Care
HIGH
FDA DRUG

Major Pharmaceuticals Recalls Prescription Medication Over Contamination Risk

Major Pharmaceuticals recalled Sulfamethoxazole and Trimethoprim tablets on September 2, 2025, due to contamination concerns. A foreign substance was found in the packaging material, although the tablets themselves remain unaffected. Consumers should stop using the product immediately and consult healthcare providers.

SULFAMETHOXAZOLE AND TRIMETHOPRIM
Presence of
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