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Medical Device

Allura Xper FD20/10; System Code: 722029;

Recall date: 2026-04-08 · Source: FDA_DEVICE
Product
Allura Xper FD20/10; System Code: 722029;
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
85 units (20 US, 65 OUS)
Description
Allura Xper FD20/10; System Code: 722029;
View official recall notice →