Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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: 5 units (OUS only) Lot/code info: System Code: 722039; UDI: 00884838054271; System Serial Number: 4, 2, 5, 8, 6;
00884838054271
Official record: FDA (Device enforcement) ↗
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