Official recall notice

FDA DeviceClass IINotable

FDA Recall: ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033;

Recall date
2026-04-08
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

2 units (1 US, 1 OUS)

Product description

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Verify with the official notice →
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