Health & Personal Care
HIGH
FDA DEVICE
Philips Philips Medical Systems Netherlands B.V. Allura Xper FD20/20 OR Table Recall Affects 3 Units
Philips Medical Systems Netherlands B.V. recalled 3 Allura Xper FD20/20 OR Tables worldwide, including the US, on 2025-09-03 after detection of degradation in internal components. The recall cites CMOS battery, hard disk drive, and/or power supply unit deterioration. Motorized movements may fail while imaging remains available. The recall is active. Stop using the device following recall guidance.
Philips Medical Systems Netherlands B.V.
Systems may