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Medical Device

Allura Xper FD20/20 OR Table; System Code: 722039;

Recall date: 2026-04-08 · Source: FDA_DEVICE
Product
Allura Xper FD20/20 OR Table; System Code: 722039;
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
5 units (OUS only)
Description
Allura Xper FD20/20 OR Table; System Code: 722039;
View official recall notice →