chemical hazard Recalls

1,035 recalls tagged with “chemical hazard”.

Health & Personal Care
HIGH
FDA DRUG

Apotex Recalls Ophthalmic Solution Over Sterility Concerns

Apotex Inc. recalled 151,034 bottles of Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution on September 5, 2025. The recall stems from a lack of assurance of sterility due to improper bottle sealing. Consumers should stop using the product immediately and contact their healthcare provider or Apotex Corp.

BRIMONIDINE TARTRATE/TIMOLOL MALEATE OPHTHALMIC SOLUTION
Lack of
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Food & Beverages
HIGH
FDA FOOD

Chetak New York Recalls Garlic Cubes Over Salmonella Risk

Chetak New York recalled over 3.5 million bags of frozen garlic cubes on September 5, 2025. The recall follows positive salmonella tests in the product. Consumers should not consume the affected garlic cubes and should seek refunds.

CHETAK NEW YORK
Product tested
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Food & Beverages
HIGH
FDA FOOD

Chetak New York Recalls Frozen Peas and Carrots for Salmonella Risk

Chetak New York recalled over 3.5 million bags of PREMIUM Select Peas and Carrots on September 5, 2025. The recall follows positive tests for Salmonella, a dangerous pathogen. Consumers should not consume the product and seek refunds immediately.

CHETAK NEW YORK
Product tested
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Health & Personal Care
HIGH
FDA DRUG

Apotex Recalls Ketorolac Ophthalmic Solution Over Sterility Concerns

Apotex Corp. recalled 493,468 bottles of Ketorolac Tromethamine Ophthalmic Solution on September 5, 2025. The recall stems from a lack of assurance of sterility due to improper bottle sealing. Consumers should stop using the product immediately and contact their healthcare provider for guidance.

KETOROLAC TROMETHAMINE
Lack of
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Food & Beverages
HIGH
FDA FOOD

Deep-brand Green Channa Recalled Due to Salmonella Risk

CHETAK NEW YORK LLC recalled over 3.5 million bags of Deep-brand PREMIUM Select Green Channa on September 5, 2025. The recall follows positive Salmonella test results. Consumers should not consume the product and seek refunds immediately.

CHETAK NEW YORK
Product tested
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Food & Beverages
HIGH
FDA FOOD

Chetak New York Recalls Chikoo Slices Due to Salmonella Risk

Chetak New York recalled 3,509,532 bags of Premium Select Chikoo Slices on September 5, 2025, after the product tested positive for Salmonella. Consumers should not consume these frozen fruit slices and should contact the company for a refund. The recall affects various lot numbers including 24356 and 25060.

CHETAK NEW YORK
Product tested
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Food & Beverages
HIGH
FDA FOOD

CHETAK NEW YORK Recalls Falsa Frozen Product Due to Salmonella Risk

CHETAK NEW YORK recalled 3,509,532 bags of PREMIUM Select Falsa KEEP FROZEN on September 5, 2025. The product tested positive for Salmonella, a serious health risk. Consumers should not consume the product and can contact the company for refunds.

CHETAK NEW YORK
Product tested
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Food & Beverages
HIGH
FDA FOOD

Chetak New York Recalls Frozen Arvi Over Salmonella Risk

Chetak New York LLC recalled over 3.5 million bags of frozen Arvi on September 5, 2025, after testing positive for Salmonella. Consumers should not consume the product due to serious health risks. The recall affects multiple lot numbers sold across the United States.

CHETAK NEW YORK
Product tested
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Food & Beverages
HIGH
FDA FOOD

Deep-brand Ponk Recalled Due to Salmonella Risk

Deep-brand recalled approximately 3.5 million bags of Ponk With Tangy Sev on September 5, 2025, after testing positive for Salmonella. The affected product weighs 6 ounces and was distributed across the United States. Consumers should stop using this product immediately and seek a refund or replacement.

CHETAK NEW YORK
Product tested
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound L17-5 Transducer Recalled for Useful-Life Labeling (2025)

Two Philips Ultrasound L17-5 transducers distributed nationwide to hospitals are recalled. The recall targets labeling that defines the devices' useful life. Stop using the transducers and follow Philips Ultrasound's instructions. Hospitals should contact Philips Ultrasound for guidance.

Philips Ultrasound
To provide
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Food & Beverages
HIGH
FDA FOOD

Chetak New York Recalls Val Papdi Due to Salmonella Risk

Chetak New York LLC recalled over 3.5 million bags of Deep-brand Select Val Papdi on September 5, 2025, after testing positive for Salmonella. The recall affects various lot numbers, prompting an immediate stop to consumption and a request for refunds or replacements.

CHETAK NEW YORK
Product tested
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Food & Beverages
HIGH
FDA FOOD

Chetak New York Recalls Jamun Over Salmonella Risk

Chetak New York LLC recalled over 3.5 million bags of PREMIUM Select Jamun on September 5, 2025, due to potential Salmonella contamination. The recall affects products distributed throughout the United States. Consumers should not consume the product and seek refunds immediately.

CHETAK NEW YORK
Product tested
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Food & Beverages
HIGH
FDA FOOD

Chetak New York Recalls Surti Papdi Due to Salmonella Risk

Chetak New York recalled over 3.5 million bags of Surti Papdi on September 5, 2025, after testing positive for Salmonella. Consumers should not consume this product and seek refunds or replacements. The recall affects bags with lot numbers 24363, 25011, and 25046.

CHETAK NEW YORK
Product tested
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Food & Beverages
HIGH
FDA FOOD

CHETAK NEW YORK Recalls Frozen Chauri Due to Salmonella Risk

CHETAK NEW YORK recalled over 3.5 million bags of Frozen Chauri on September 5, 2025, after testing positive for Salmonella. Consumers should not eat the product and seek a refund or replacement. The recall affects products distributed throughout the United States.

CHETAK NEW YORK
Product tested
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Food & Beverages
HIGH
FDA FOOD

Deep-brand Diced Bottle Gourd Recalled Due to Salmonella Risk

Deep-brand PREMIUM Select Dudhi (Lauki) Diced Bottle Gourd has been recalled after testing positive for Salmonella. The recall affects 3,509,532 bags distributed in the United States. Consumers should refrain from consuming the product and seek a refund or replacement.

CHETAK NEW YORK
Product tested
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Health & Personal Care
HIGH
FDA DRUG

Zydus Pharmaceuticals Recalls Entecavir Tablets Over Impurity Risk

Zydus Pharmaceuticals recalled 4,440 bottles of Entecavir Tablets on September 4, 2025. The recall follows failure to meet impurity and degradation specifications. Consumers should stop using the affected tablets immediately and contact their healthcare provider.

Zydus Pharmaceuticals USA Inc.
Failed Impurity/Degradation
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