All Product Recalls

Browse through 2,313 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

HIGHFDA 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
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HIGHFDA 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
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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
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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
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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
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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.

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HIGHFDA 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
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HIGHFDA FOOD

Chetak New York Recalls Frozen Carrots Due to Salmonella Risk

Chetak New York recalled 3.5 million bags of frozen sliced carrots on September 5, 2025, after testing positive for Salmonella. The recall affects products sold across the United States. Consumers should not eat the recalled items and seek refunds immediately.

CHETAK NEW YORK
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HIGHFDA FOOD

Chetak New York Recalls Diced Green Mango Over Salmonella Risk

Chetak New York LLC recalled over 3.5 million bags of PREMIUM Select Diced Green Mango on September 5, 2025. The product tested positive for Salmonella, posing a serious health risk to consumers. The recall affects products distributed across the United States.

CHETAK NEW YORK
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HIGHFDA FOOD

Chetak New York Recalls Surti Undhiu Mix Due to Salmonella Risk

Chetak New York recalled over 3.5 million bags of Surti Undhiu Mix on September 5, 2025, after the product tested positive for Salmonella. The recall affects multiple lot numbers of the 12 oz. frozen vegetable mix distributed across the United States.

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 DEVICE

Spacelabs Healthcare Recalls DVI Display Cables Over Safety Risk

Spacelabs Healthcare recalled 16,898 DVI display cables on September 5, 2025. The cables may not comply with electromagnetic interference standards, posing risks to patient safety. Healthcare providers and patients must stop using these cables immediately.

Spacelabs Healthcare
Due to
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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

Chetak New York Recalls Garlic Cloves for Salmonella Risk

Chetak New York recalled 3.5 million bags of frozen garlic cloves on September 5, 2025, due to potential Salmonella contamination. The recall affects products sold across the United States. Consumers should not consume the product and seek a refund.

CHETAK NEW YORK
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Recalled AR-15 Chamber Lock Pro (Red)
HIGH
CPSC

StopBox USA Recalls AR-15 Chamber Lock Pro Due to Injury Risk

StopBox USA recalled AR-15 Chamber Lock Pro firearm locks on September 4, 2025. A manufacturing defect allows unauthorized access to firearms, posing a risk of serious injury or death. Consumers should immediately stop using the locks and contact StopBox for refunds or replacements.

StopBox USA
A manufacturing
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