FDA DeviceClass IINotable
FDA Recall: ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;
Description
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Hazard
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Remedy
5084 units (1616 US, 3468 OUS)
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