PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033;

Hazard

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Details from the source

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. Distribution: Domestic: Nationwide Distribution; International: Afghanistan, Albania, Algeria, Argentina, Armenia, Australia, Austria, Bahamas, Bahrain, Bangladesh, Belarus, Belgium, Bolivia, Bosnia and Herzegovina, Botswana, Brazil, Brunei Darussal, Bulgaria, Cambodia, Canada, Cayman Islands, Chile, China, Colombia, Costa Rica, C¿te D'Ivoire, Croatia, Cuba, Cyprus, Czech Republic, Denmark, Dominican Republic, Quantity: 2 units (1 US, 1 OUS) Lot/code info: (1) System Code: 722022; UDI: 00884838059078; System Serial Number: 6; (2) System Code: 722033; UDI: 00884838054233; System Serial Number: 1;

UPC codes

00884838059078, 00884838054233

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.