All Product Recalls

Browse through 1,551 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

HIGHFDA 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
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HIGHFDA 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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HIGHFDA 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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HIGHFDA FOOD

Deep-brand Lotus Root Recalled for Salmonella Risk

CHETAK NEW YORK recalled over 3.5 million bags of PREMIUM Select Lotus Root on September 5, 2025. The product tested positive for Salmonella, posing a serious health risk. Consumers should stop using the product immediately and seek refunds.

CHETAK NEW YORK
Product tested
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HIGHFDA FOOD

Chetak New York Recalls Sambhar Mix Due to Salmonella Risk

Chetak New York recalled over 3.5 million bags of Premium Select Sambhar Mix on September 5, 2025, after testing positive for Salmonella. Consumers should not eat the product and must seek refunds. The recall affects specific lot numbers sold across the United States.

CHETAK NEW YORK
Product tested
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HIGHFDA 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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HIGHFDA DEVICE

GE Medical Systems Recalls AW Server Models Over Data Security Risk

GE Medical Systems recalled 7,302 AW Server units on September 5, 2025, due to a critical security vulnerability. The flaw could allow unauthorized access to sensitive patient data. Healthcare providers and patients must cease use immediately and follow recall procedures.

GE Medical Systems
Firm has
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HIGHFDA 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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HIGHFDA FOOD

Chetak New York Recalls Hot Green Chillies Over Salmonella Risk

Chetak New York recalled over 3.5 million bags of PREMIUM Select Hot Green Chillies on September 5, 2025. The product tested positive for Salmonella, a bacteria that can cause serious illness. Consumers should not eat the product and should seek a refund or replacement immediately.

CHETAK NEW YORK
Product tested
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HIGHFDA FOOD

Deep-brand Sweet Corn Recalled for Salmonella Contamination

Deep-brand recalled 3.5 million bags of PREMIUM Select Sweet Corn on September 5, 2025, due to Salmonella contamination. The affected product weighs 2 pounds and was distributed across the United States. Consumers should not consume this product and should seek a refund.

CHETAK NEW YORK
Product tested
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HIGHFDA FOOD

Chetak New York Recalls Frozen Vegetables Due to Salmonella Risk

Chetak New York LLC recalled over 3.5 million bags of frozen mixed vegetables on September 5, 2025, due to Salmonella contamination. Consumers should not eat the product and should seek refunds or replacements. The recall affects products distributed across the United States.

CHETAK NEW YORK
Product tested
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HIGHFDA FOOD

Chetak New York Recalls Frozen Methi Blocks Over Salmonella Risk

Chetak New York LLC recalled over 3.5 million bags of Premium Select Methi Blocks on September 5, 2025. The product tested positive for Salmonella, a serious foodborne pathogen. Consumers should not eat this product and should seek a refund or replacement.

CHETAK NEW YORK
Product tested
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HIGHFDA FOOD

Chetak New York Recalls Frozen Red Pearl Onions Due to Salmonella Risk

Chetak New York recalled over 3.5 million bags of frozen red pearl onions on September 5, 2025, after testing positive for Salmonella. The recall affects the 12 oz. packages sold across the United States. Consumers should not eat the product and should seek refunds or replacements.

CHETAK NEW YORK
Product tested
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HIGHFDA FOOD

Chetak New York Recalls Frozen Baby Bhindi Over Salmonella Risk

Chetak New York LLC recalled over 3.5 million bags of frozen baby bhindi on September 5, 2025, due to potential Salmonella contamination. The recall affects the Deep-brand Premium Select Baby Bhindi, weighing 12 oz. Consumers should not consume this product and seek refunds immediately.

CHETAK NEW YORK
Product tested
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HIGHFDA FOOD

Chetak New York Recalls Instant Stuffing for Pani Puri Over Salmonella Risk

Chetak New York LLC recalled over 3.5 million bags of Instant Stuffing for Pani Puri on September 5, 2025, due to Salmonella contamination. Consumers should not consume the product and seek a refund or replacement. The recall affects specific lots totaling 3,509,532 bags distributed across the United States.

CHETAK NEW YORK
Product tested
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