Z-1666-2026

Class II · Ongoing

Recalling firm
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Classification
Class II
Status
Ongoing
Initiated
20260303
Firm location
Best, Netherlands

Product description

ALLURA Xper FD20 Biplane OR Table; System Code: (1) 722020, (2)722025;

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.