Browse through 2,852 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Beckman Coulter recalled the UniCel DxH 600 Cellular Analysis System on August 13, 2025. The devices may produce erroneously high hemoglobin results in patients with elevated white blood cell counts. This recall affects medical facilities worldwide, including the United States.
Philips recalled 14 Brilliance iCT SP CT systems on August 13, 2025. The patient support table may descend unexpectedly due to a component misalignment. The recall affects devices distributed worldwide, including the US and 49 other countries.
Philips recalled 73 CT systems on August 13, 2025, due to a risk of the patient support table descending unexpectedly. The recall affects models 728240, 728246, and 728256 distributed worldwide. This recall includes systems sold across the US and several countries globally.
Philips recalled 181 CT scanner units on August 13, 2025, due to a risk of the patient support table descending unexpectedly. The recall affects models 728235, 728231, and 728317 distributed worldwide. Healthcare providers and patients must stop using these devices immediately to ensure safety.
Philips recalled 24 CT systems on August 13, 2025, due to a risk of the patient support table descending unexpectedly. The issue stems from a misalignment in a component after replacement. Health providers must stop using these devices immediately.
Philips recalled 285 CT systems on August 13, 2025, due to a risk of patient support tables descending unexpectedly. The recall affects model numbers 728321, 728323, and 728326. Users should stop using the devices immediately and follow manufacturer instructions.
Philips recalled three Ingenuity CT Family systems on August 13, 2025, due to a hazard that could lead to sudden descent. The issue stems from a ball screw misalignment affecting the patient support table. Users should stop using the devices immediately and follow recall instructions.
Fresh & Ready Foods LLC recalled 233 units of Tuscan Artichoke and Mozzarella Salad on August 13, 2025. The recall stems from undeclared wheat and milk allergens in ready-to-eat sandwiches. The affected products were distributed to 15 locations in California.
Fresh & Ready Foods LLC recalled 233 units of Spanish Club Ciabatta sandwiches on August 13, 2025. The recall stems from undeclared allergens, specifically wheat and milk, posing a high risk to consumers. The products were available at 15 corporate locations across California.
Philips recalled 210 Brilliance iCT CT systems on August 13, 2025. A misalignment in the ball screw may cause the patient support table to descend unexpectedly. Patients and healthcare providers must stop using the device immediately.
Philips recalled 81 IQon Spectral CT systems on August 13, 2025, due to a potential fall hazard. The patient support table may descend unexpectedly due to a ball screw misalignment. Healthcare providers and patients must stop using the device immediately.
The device does not bear a unique device identifier.
The device does not bear a unique device identifier.
The device does not bear a unique device identifier.
The device does not bear a unique device identifier.
The device does not bear a unique device identifier.
The device does not bear a unique device identifier.
The device does not bear a unique device identifier.
Change Healthcare recalled 12 programs of its Radiology Solutions software version 14.2.2 on August 13, 2025. A software issue may prevent radiology reports from displaying fully. Healthcare providers and patients must stop using the software immediately.
The device does not bear a unique device identifier.