FDA DeviceClass IINotable
FDA Recall: Allura Xper FD20/20; System Code: 722038;
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
111 units (31 US, 80 OUS)
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