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Medical Device

Allura Xper FD20/15; System Code: 722058;

Recall date: 2026-04-08 · Source: FDA_DEVICE
Product
Allura Xper FD20/15; System Code: 722058;
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
296 units (68 US, 228 OUS)
Description
Allura Xper FD20/15; System Code: 722058;
View official recall notice →