Browse through 2,852 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
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.
GE Healthcare recalled 2,306 CSCS V3 MAS800 Central Station desktops worldwide after identifying a software fault that can trigger a continuous reboot cycle. The issue can result in a loss of central monitoring for connected patients. Hospitals should stop using the affected devices and follow the recall instructions from GE HealthCare and Wipro GE Healthcare Private Ltd.
Philips Ultrasound, Inc. recalled 41 S4-1 Ultrasound Transducers distributed nationwide in the United States. The recall is to provide clarification and labeling to define the useful life of ultrasound transducers in the field. Healthcare providers should stop using these devices immediately and follow the recall instructions from Philips or their facility.
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.
Spacelabs Healthcare recalls 8,179 DVI display cables worldwide after EMI interference could affect medical monitors. The cables connect 6-foot DVI-I to DVI-I devices used with the 91390 and 91393 monitors. Healthcare providers should stop using affected cables and follow recall instructions.
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 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 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.
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 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 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.
Deep-brand Premium Select Karela Ring Cut recalled over Salmonella contamination. The recall affects 3,509,532 bags sold in the U.S. Consumers should not consume the product.
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 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 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 LLC recalled 3,509,532 bags of frozen turmeric on September 5, 2025, after testing positive for Salmonella. The affected product is labeled as Deep-brand PREMIUM Select Turmeric Yellow Haldi. Consumers should not eat this product and should contact the company for a refund or replacement.
CHETAK NEW YORK LLC recalled over 3.5 million bags of Deep-brand PREMIUM Select Amla on September 5, 2025, due to a positive Salmonella test. This Class I recall affects frozen products sold across the United States. Consumers should not consume the product and seek refunds or replacements immediately.
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 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 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.