These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
2,775 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
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.
Philips North America has issued a recall for 81 IQon Spectral CT systems, Model 728332, sold worldwide. The patient support table may descend unexpectedly to the lowest position due to ball screw misalignment after a replacement. Stop using the device immediately and follow manufacturer recall instructions.
Beckman Coulter recalled hematology analyzers configured with HGB photometers after reports of erroneously high hemoglobin results in samples with elevated WBC counts. The recall covers DxH 900 systems worldwide. Stop using the device immediately and follow manufacturer instructions. Contact Beckman Coulter or a healthcare provider for guidance.
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 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 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.
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 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.
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 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 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 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 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.
Baker's Authority recalls 197 units of Everything Bagel Mix after undeclared sesame and other ingredients. The product label failed to list sesame and other ingredients. Consumers who bought the mix should not consume it and should seek a refund or replacement.
Viona Pharmaceuticals recalls Tavaborole Topical Solution 5% 10 mL bottles, distributed nationwide in the U.S. The effective recall date is August 12, 2025. The product is manufactured by Zydus Lifesciences Ltd. Discoloration was cited as the reason for the recall. Consumers should stop using the product and contact the distributor for guidance.
Wegmans Food Markets recalled 4,884 units of Medium Camembert Soft Ripened Cheese on August 12, 2025. The product may be contaminated with Listeria monocytogenes, posing a serious health risk. Consumers should not eat the cheese and should contact the company for refunds.
Baker’s Authority recalled 70 units of Graham Cracker Meal on August 12, 2025. The product ships to multiple states. Undeclared wheat and soy allergens are listed on the label. The recall urges consumers to avoid consumption and seek refunds or replacements.
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.
Max Mobility LLC recalls 8,413 Smart Drive MX2+ SpeedControl Dials used with the SmartDrive MX2+ Wheelchair Power Assist. A faulty electrical connection between the dial and the motor can cause loss of control. Stop using the device immediately and follow recall letters for instructions.