immediate action Recalls

2,756 recalls tagged with “immediate action”.

Food & Beverages
HIGH
FDA 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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Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound C9-4 Transducer Recalled for Lifespan Labelling — 1 Unit (2025)

Philips Ultrasound recalled 1 unit of the C9-4 Ultrasound Transducer, Model No. 989605365021, distributed nationwide in the United States. The recall focuses on clarifying and labeling the device’s useful life. Healthcare providers and patients should stop using the device immediately and follow Philips’ instructions for replacement or further steps.

Philips Ultrasound
To provide
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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
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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
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Health & Personal Care
HIGH
FDA DRUG

Endo USA Recalls 1,041 Cartons of Everolimus 5mg Tablets Over IP-C Impurity (2025)

Endo USA, Inc. recalled 1,041 cartons of Everolimus 5mg tablets nationwide in the United States due to an impurity IP-C out of specification. The impurity IP-C is out of specification in the drug product. Patients and healthcare providers should stop using this product immediately and contact Endo USA or their healthcare provider for guidance.

Everolimus
Failed Impurities/Degradation
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Health & Personal Care
LOW
FDA DEVICE

Philips 3D6-2 Ultrasound Transducer Recalled for Labeling Clarification (17 Units, 2025)

Philips recalled 17 units of the 3D6-2 Ultrasound Transducer distributed nationwide to healthcare facilities in the United States. The recall seeks to clarify labeling defining the transducer’s useful life. Clinicians and facilities should stop using the device immediately and follow Philips recall instructions.

Philips Ultrasound
To provide
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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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Food & Beverages
HIGH
FDA FOOD

Chetak New York Issues Salmonella Recall for Frozen Surti Papdi Lilva

Chetak New York recalled over 3.5 million bags of Premium Select Surti Papdi Lilva on September 5, 2025, due to Salmonella contamination. Consumers should not eat the product and seek refunds immediately. The recall affects multiple lot numbers sold across the United States.

CHETAK NEW YORK
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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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Food & Beverages
HIGH
FDA FOOD

Chetak New York Recalls Frozen Tindora Due to Salmonella Risk

Chetak New York announced a recall of 3,509,532 bags of Deep-brand Select Tindora on September 5, 2025. The product tested positive for Salmonella, a serious foodborne pathogen. Consumers should not consume the product and seek a refund or replacement immediately.

CHETAK NEW YORK
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Food & Beverages
HIGH
FDA FOOD

Chetak New York Recalls Frozen Punjabi Tinda Due to Salmonella Risk

Chetak New York LLC recalled 3.5 million bags of frozen Punjabi Tinda on September 5, 2025, after testing positive for Salmonella. Consumers should not eat the product, as it poses a serious health risk. The recall affects various lot numbers and was issued in the United States.

CHETAK NEW YORK
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Food & Beverages
HIGH
FDA FOOD

Chetak New York Recalls Frozen Okra Due to Salmonella Risk

Chetak New York recalled over 3.5 million bags of frozen okra on September 5, 2025, after tests revealed contamination with Salmonella. Consumers should not eat the product and seek refunds or replacements. The recall affects multiple lot numbers sold across the United States.

CHETAK NEW YORK
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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

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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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 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
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Food & Beverages
HIGH
FDA FOOD

Chetak New York Recalls Frozen Yams Due to Salmonella Risk

Chetak New York recalled over 3.5 million bags of frozen yams on September 5, 2025, after testing positive for Salmonella. Consumers should not eat these products, which may pose a serious health risk. The recall affects specific lot numbers of the Deep-brand Premium Select Ratalu Sliced Violet Indian Yams.

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
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