All Product Recalls

Browse through 2,852 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

Health & Personal Care
HIGH
FDA DEVICE

Philips X7-2 Ultrasound Transducer Recall for 5 Units Nationwide (2026)

Philips Ultrasound recalled 5 X7-2 ultrasound transducers distributed nationwide to healthcare providers. The recall is to provide clarification and labeling to define the useful life of ultrasound transducers in the field. Healthcare facilities should stop using the recalled devices and follow Philips Ultrasound, Inc instructions or contact their provider for guidance.

Philips Ultrasound
To provide
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound Recalled 11 Mini Multi TEE Transducers Over Useful-Life Labeling (2025)

Philips Ultrasound recalled 11 Mini Multi TEE ultrasound transducers distributed nationwide in the United States after a labeling clarification related to useful life. The recall centers on providing clarification and labeling to define the useful life of transducers in the field. Healthcare providers should stop using the device and follow recall instructions from Philips Ultrasound, Inc or their

Philips Ultrasound
To provide
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Food & Beverages
HIGH
FDA FOOD

Deep-brand Frozen French Beans Recalled Due to Salmonella Risk

Deep-brand PREMIUM Select Fansi Cut French Beans have been recalled after testing positive for Salmonella. The recall affects approximately 3,509,532 bags distributed across the United States. Consumers should not consume the product and seek a refund immediately.

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

Apotex Ketorolac Tromethamine Ophthalmic Solution Recall 2025: 493,468 Bottles Nationwide

Apotex Corp. is recalling 493,468 bottles of Ketorolac Tromethamine Ophthalmic Solution, 0.5%, Rx Only, sterile, distributed nationwide in the United States. The recall cites lack of assurance of sterility due to improper bottle sealing. Consumers and healthcare providers should stop using the product immediately and contact Apotex Corp. or their healthcare provider for guidance.

Apotex
Lack of
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound X3-1 Transducer Recalled for Labeling Clarification in 2026 (17 Units)

Philips Ultrasound recalled 17 X3-1 ultrasound transducers nationwide in the United States. The recall is to provide clarification and labeling to define the useful life of transducers in the field. Healthcare providers and patients should stop using the affected devices immediately and await further manufacturer instructions.

Philips Ultrasound
To provide
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Food & Beverages
HIGH
FDA FOOD

CHETAK NEW YORK Recalls Amla Slices Due to Salmonella Risk

CHETAK NEW YORK recalled over 3.5 million bags of Premium Select Amla Slices on September 5, 2025, after testing positive for Salmonella. Consumers should not consume this product and seek refunds or replacements. The recall affects various lot numbers sold across the United States.

CHETAK NEW YORK
Product tested
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Food & Beverages
HIGH
FDA FOOD

Chetak New York Recalls Frozen Guvar Due to Salmonella Risk

Chetak New York LLC recalled over 3.5 million bags of frozen Guvar on September 5, 2025, after testing positive for Salmonella. The recall affects products sold in the United States. Consumers should not consume the recalled product and seek a refund or replacement immediately.

CHETAK NEW YORK
Product tested
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Food & Beverages
HIGH
FDA FOOD

Chetak New York Recalls Frozen Water Chestnuts for Salmonella Risk

Chetak New York recalled over 3.5 million bags of frozen water chestnuts on September 5, 2025, after testing positive for Salmonella. The recall affects the PREMIUM Select Singoda (Cooked) Water Chestnuts, weighing 12 oz. each. Consumers should not consume the product and seek a refund or replacement.

CHETAK NEW YORK
Product tested
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Food & Beverages
HIGH
FDA FOOD

CHETAK NEW YORK Recalls Frozen Suran Over Salmonella Risk

CHETAK NEW YORK recalled 3,509,532 bags of its Premium Select Suran on September 5, 2025. The product tested positive for Salmonella, posing a serious health risk to consumers. Customers should stop using the product immediately and seek a refund or replacement.

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 Green Chili Due to Salmonella Risk

Chetak New York recalled over 3.5 million bags of frozen green chili on September 5, 2025. The product tested positive for Salmonella, a serious foodborne pathogen. 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 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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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

CHETAK NEW YORK Recalls Frozen Garlic Over Salmonella Risk

CHETAK NEW YORK recalled 3,509,532 bags of PREMIUM Select Green Garlic on September 5, 2025, after testing positive for Salmonella. The recall affects products distributed throughout the United States. Consumers should not eat the product and should seek a refund or replacement.

CHETAK NEW YORK
Product tested
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Food & Beverages
HIGH
FDA FOOD

CHETAK NEW YORK Recalls Dum Aloo Due to Salmonella Risk

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

CHETAK NEW YORK
Product tested
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Food & Beverages
HIGH
FDA FOOD

CHETAK NEW YORK Recalls Frozen Peas Over Salmonella Risk

CHETAK NEW YORK recalled over 3.5 million bags of frozen peas on September 5, 2025, after testing positive for Salmonella. The recall affects multiple lot numbers and poses a high health risk to consumers. The company urges anyone who purchased the product to stop using it immediately.

CHETAK NEW YORK
Product tested
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Food & Beverages
HIGH
FDA FOOD

CHETAK NEW YORK Recalls Frozen Vegetables for Salmonella Risk

CHETAK NEW YORK LLC recalled 3,509,532 bags of Deep-brand Premium Select Kantola on September 5, 2025. The recall follows a positive test for Salmonella, posing a serious health risk. Consumers should not consume the product and should seek a refund.

CHETAK NEW YORK
Product tested
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Food & Beverages
HIGH
FDA FOOD

CHETAK NEW YORK Recalls Frozen Tuvar Lilva Over Salmonella Risk

CHETAK NEW YORK recalled over 3.5 million bags of PREMIUM Select Tuvar Lilva on September 5, 2025, due to Salmonella contamination. Consumers should not eat the product and can seek refunds or replacements. The recall affects products distributed across the United States.

CHETAK NEW YORK
Product tested
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Food & Beverages
HIGH
FDA 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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