Official recall notice
FDA DeviceClass IINotable
FDA Recall: Allura Xper FD20/20 OR Table; System Code: 722039;
- Recall date
- 2026-04-08
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Recommended action
What to do
5 units (OUS only)
Product description
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.