Medical Device

Allura Xper FD20/20; System Code: 722038;

Recall date: 2026-04-08 · Source: FDA_DEVICE

Brand / Firm

Product

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

111 units (31 US, 80 OUS)

Description

Allura Xper FD20/20; System Code: 722038;