Official recall notice

FDA DeviceClass IINotable

FDA Recall: Allura Xper FD20/10; System Code: 722029;

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

85 units (20 US, 65 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 →
Share:

Related Recalls

2026-08-19 · FDA_DEVICE
FDA Recall: Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058. In
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
2026-08-19 · FDA_DEVICE
FDA Recall: Philips Azurion, Model Numbers: 722229, 722230, 722231, 722232, 722233, 722234, 722235, and 722236,
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
2026-08-19 · FDA_DEVICE
FDA Recall: Philips Azurion Rystem, Model Numbers: 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
2026-08-12 · FDA_DEVICE
FDA Recall: Philips Allura, Cardio Vascular-Allura Centron. Model Number: 722400. Interventional Fluoroscopic
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.