Browse through 2,852 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
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.
Philips Ultrasound recalled 1 unit of the S5-2 Ultrasound Transducer sold nationwide through healthcare distributors. The recall clarifies labeling to define the useful life of the transducer in the field. Healthcare providers should stop using the device and contact Philips Ultrasound for instructions.
Two Philips Ultrasound L17-5 transducers distributed nationwide to hospitals are recalled. The recall targets labeling that defines the devices' useful life. Stop using the transducers and follow Philips Ultrasound's instructions. Hospitals should contact Philips Ultrasound for guidance.
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.
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.
Spacelabs Healthcare has recalled 820 DVI display cables worldwide due to shielding issues that may cause electromagnetic interference with other medical devices. The cables connect monitors used in patient care. Hospitals should stop using the affected cables and follow manufacturer recall instructions. The recall was issued by letter and is active as of 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 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.
CHETAK NEW YORK recalled 3,509,532 bags of its PREMIUM Select Snake Gourd on September 5, 2025. The product tested positive for Salmonella, posing a serious health risk. Consumers should not eat the product and seek refunds.
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.
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 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.
Spacelabs Healthcare is recalling 16,898 DVI display cables worldwide, including the United States. The cables are used as external display connectors for certain monitors. The recall follows a risk that inadequately shielded cables may cause electromagnetic interference with other medical devices. Stop using the affected cables immediately and await manufacturer instructions.
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.
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 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 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 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.
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.
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.