Browse through 2,852 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Philips recalled 14 Brilliance iCT SP CT systems, model 728311, sold worldwide including the United States. The patient support couch may descend unexpectedly to the lowermost position because of ball screw misalignment after a replacement. Hospitals should stop using the device immediately and await manufacturer instructions.
Philips North America recalls 210 CT systems worldwide after reports that the patient support couch may descend unexpectedly to the lowest position following a replacement. Philips issued a recall dated 2025-08-13 with active status. The recall number is Z-2598-2025. Stop using immediately and follow manufacturer instructions.
Fresh & Ready Foods recalled 233 units of Tuscan Artichoke and Mozzarella Salad distributed to 15 California locations after undeclared wheat and milk allergens were found. The allergen was not declared on the label. Consumers should not eat the product and should contact Fresh & Ready Foods LLC for refunds or replacements via email.
Fresh & Ready Foods recalled 233 Spanish Club Ciabatta sandwiches sold to 15 California locations after discovering undeclared wheat and milk allergens. The recall is Class I and the hazard is an undisclosed allergen on ready-to-eat sandwiches. Consumers should not eat the sandwiches and should contact Fresh & Ready Foods for refunds or replacements by email.
Beckman Coulter recalled the UniCel DxH 690T COULTER Cellular Analysis System configured with the LED HGB Photometer REF C34520. The hematology analyzer may produce erroneously high hemoglobin results on samples with elevated white blood cell counts. Labs should stop using the device immediately and follow Beckman Coulter's recall instructions.
Fresh & Ready Foods recalled 233 Piccolo Pranzo Box sandwiches after undeclared wheat and milk allergens were detected. The product was distributed to 15 California locations. Consumers should not eat the product and should contact Fresh & Ready Foods for refund or replacement information via email.
Novartis Manufacturing NV and Sandoz Inc recall ciprofloxacin 0.3% and dexamethasone 0.1% otic suspension after temperature abuse. The recall affects one consignee in California. Consumers and health care providers should stop using the product immediately and follow guidance from Sandoz or a healthcare provider.
Philips recalled 24 CT systems worldwide after finding that the patient support couch may descend unexpectedly following a replacement. The defect involves a misaligned ball screw in the couch mechanism. Hospitals and imaging centers should stop using the device immediately and follow Philips recall instructions.
Penner Patient Care recalled 15 Penner Pacific Bathing Spa devices distributed nationwide to healthcare providers in the United States. The devices do not bear a unique device identifier. Stop using the device immediately and follow recall instructions from the manufacturer or your healthcare provider.
Penner Patient Care recalled 45 Penner Pacific Bathing Spa units distributed nationwide in the United States. The devices do not bear a unique device identifier. Patients and healthcare providers should stop using this device immediately and follow the recall instructions provided by the manufacturer.
Change Healthcare recalled 12 programs of its Radiology Solutions software version 14.2.2 after reports surfaced that radiology reports may not display completely. This software flaw could lead to incomplete medical assessments and potential health risks. Healthcare providers and patients should stop using the software immediately and follow the recall instructions.
Penner Patient Care recalled 643 devices nationwide after the FDA flagged missing unique device identifiers. The recall affects a broad range of Penner Pacific Bathing Spa models. The device lacks a unique device identifier, posing regulatory and traceability concerns. Stop using the device and follow recall instructions from Penner Patient Care or a healthcare provider.
Penner Patient Care, Inc. recalled 21 Penner Pacific Bathing Spa units distributed nationwide in the United States after discovering the devices do not bear a unique device identifier. The missing UDI hinders traceability for adverse events and recalls. Consumers should stop using the devices and contact Penner Patient Care for instructions.
Penner Patient Care recalled 26 Penner Pacific Bathing Spa units distributed nationwide in the United States after finding they do not bear a unique device identifier. The absence of a UDI prevents reliable traceability of the devices. Healthcare providers and patients should stop using the devices and follow the manufacturer’s recall instructions.
Penner Patient Care recalled 25 Penner Pacific Bathing Spas nationwide after confirming the device does not bear a unique device identifier. The missing UDI impedes traceability and oversight. Stop using the device and follow the manufacturer’s recall instructions.
Penner Patient Care recalls 190 Bathing Spa devices nationwide after discovering the units lack a unique device identifier. The issue involves missing UDI on the device. Stop using the device immediately and follow the recall instructions.
Penner Patient Care recalls 206 US units of the Penner Pacific Bathing Spa after the device lacks a unique device identifier. The recall targets models listed with multiple variations and serial numbers. Consumers should stop using the device immediately and follow manufacturer instructions.
Penner Patient Care recalled 10 Penner Pacific Bathing Spa units nationwide on 2025-08-13 after regulators flagged the device lacks a unique device identifier. The device does not bear a unique device identifier. Patients and healthcare providers should stop using the device immediately and follow the manufacturer’s recall instructions.
Penner Patient Care recalled 158 Penner Pacific Bathing Spa devices distributed nationwide in the United States. The device does not bear a unique device identifier. Healthcare providers and patients should stop using the device immediately and follow the recall instructions mailed to affected parties.
Wegmans Food Markets recalled 4,884 units of Caramel Apple Pecan Topped Brie Cheese on August 12, 2025. The cheese may be contaminated with Listeria monocytogenes, a serious pathogen. Consumers should not consume this product and seek a refund.