2,756 recalls tagged with “immediate action”.
GE Medical Systems recalled 1,818 Senographe Pristina mammography systems on October 24, 2025. The recall affects systems due to missing or incorrect X-Ray Warning labels. This nonconformance to FDA regulations poses a high hazard risk.
Bio Ionic recalls the 1-Inch-Long Barrel Curling Iron model LXT-CL-1.0 with date code 0722-1223. The recall is active as of 2025-10-23. Consumers should stop using the recalled curling iron and contact Bio Ionic for a free replacement.
LEACHOI recalled its adult portable bed rails sold on Amazon on Oct. 23, 2025. The recall covers ASIN B0BZVCG2R5 due to a risk of entrapment and suffocation and missing hazard labels. Stop using the recalled rails and seek a full refund from LEACHOI.
Firm is initiating a removal due to continued reports of adverse events.
Olympus Corporation recalled 3,381 units of the Thunderbeat surgical instrument on October 22, 2025. The recall follows continued reports of adverse events associated with the device. Patients and healthcare providers must stop using the product immediately.
Olympus Corporation of the Americas recalled 140 units of its Thunderbeat surgical device on October 22, 2025. Users reported ongoing adverse events linked to the device. Healthcare providers should stop using it immediately and follow recall instructions.
Firm is initiating a removal due to continued reports of adverse events.
Firm is initiating a removal due to continued reports of adverse events.
Firm is initiating a removal due to continued reports of adverse events.
Firm is initiating a removal due to continued reports of adverse events.
Firm is initiating a removal due to continued reports of adverse events.
Firm is initiating a removal due to continued reports of adverse events.
Firm is initiating a removal due to continued reports of adverse events.