Allura Xper FD20/10 X-ray systems recalled for BIOS battery startup failure
Philips is recalling 87 Allura Xper FD20/10 interventional X-ray systems because the BIOS battery may deplete faster than designed, halting start-up.
- Product
- Allura Xper FD20/10; Model Numbers: 722029; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;
- Category
- Medical Device
- Distribution
- Distributed nationwide