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Medical Device

ALLURA Xper FD10F; System Code: 722002;

Recall date: 2026-04-08 · Source: FDA_DEVICE
Product
ALLURA Xper FD10F; System Code: 722002;
Reason for recall
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Units affected
10 units (8 US, 2 OUS)
Description
ALLURA Xper FD10F; System Code: 722002;
View official recall notice →