Philips North America Llc recalls DigitalDiagnost C90 Flex/Value/Chest/ER, used to acquire, pr
Recalled Product
DigitalDiagnost C90 Flex/Value/Chest/ER, used to acquire, process, store, display and export digital radiographic images.
Hazard / Issue
Potential for units suspended on the ceiling to fail and fall.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Model No. 712035; UDI: (01)00884838090705(21)10000009, (01)00884838090705(21)10000010, (01)00884838090705(21)10000003, (01)00884838090705(21)10000004, (01)00884838090705(21)10000002, (01)00884838090705(21)10000001, (01)00884838090705(21)10000053 , (01)00884838090705(21) 10001042 , (01)00884838090705(21) 10001044 , (01)00884838090705(21) 10001125 , (01)00884838090705(21) 10001113 , (01)00884838090705(21) 10001111 , (01)00884838090705(21) 10001112 , (01)00884838090705(21) 10001109 , (01)00884838090705(21) 10001110 , (01)00884838090705(21) 10001114 , (01)00884838090705(21) 21862107 , (01)00884838090705(21) 10001130 , (01)00884838090705(21) 21862103 , (01)00884838090705(21) 21862101 , (01)00884838090705(21) 21862100 , (01)00884838090705(21) 22860370 , (01)00884838090705(21) 21862123 , (01)00884838090705(21) 21862126 , (01)00884838090705(21) 22860323 , (01)00884838090705(21) 22860045 , (01)00884838090705(21) 22860317 , (01)00884838090705(21) 22860316 , (01)00884838090705(21) 22860318 , (01)00884838090705(21) 22860342 , (01)00884838090705(21) 22860357 , (01)00884838090705(21) 23860320 , (01)00884838090705(21) 23860316; Serial No. 10000009, 10000010, 10000003, 10000004, 10000002, 10000001, 10000053, 10001042, 10001044, 10001125, 10001113, 10001111, 10001112, 10001109, 10001110, 10001114, 21862107, 10001130, 21862103, 21862101, 21862100, 22860370, 21862123, 21862126, 22860323, 22860045, 22860317, 22860316, 22860318, 22860342, 22860357, 23860320, 23860316.
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