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.
HEB recalled 468 cases of Blueberry Flavored Yogurt Pretzels on August 13, 2025. The recall affects 8oz packages with UPC code 9787011400 due to undeclared wheat allergen. Consumers should stop consuming the product 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.
Beckman Coulter recalled the UniCel DxH 690T COULTER Cellular Analysis System on August 13, 2025. Erroneously high hemoglobin results may occur in patients with elevated white blood cell counts. Healthcare providers and patients must stop using the device immediately.
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.
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 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.
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.
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.
The device does not bear a unique device identifier.
Baker's Authority recalled 78 units of Three Seed Mix on August 12, 2025. The product lacks proper labeling for sesame, a major allergen. Consumers should not consume this product and seek a refund.
Max Mobility recalled 25,389 Smart Drive MX2+ SpeedControl Dials on August 12, 2025. A faulty electrical connection can lead to loss of control, posing injury risks. Users must stop using the device immediately and follow recall instructions.
Viona Pharmaceuticals recalled 3,960 bottles of Tavaborole Topical Solution on August 12, 2025. The product may show discoloration, posing health risks to consumers. This recall affects topical solutions distributed nationwide in the USA.