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ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033;

Recall date: 2026-04-08 · Source: FDA_DEVICE
Product
ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033;
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
2 units (1 US, 1 OUS)
Description
ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033;
View official recall notice →