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GE OEC 9800 Adverse Event — Malfunction (MDR 1720753-2008-16303)

GE OEC 9800 Adverse Event — Malfunction (MDR 1720753-2008-16303) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: GE OEC 9800; Generic name: FLUOROSCOPIC X-RAY; Manufacturer: GE OEC MEDICAL SYSTEMS INC..

DeviceGE OEC 9800
Generic nameFLUOROSCOPIC X-RAY
ManufacturerGE OEC MEDICAL SYSTEMS INC.
Report number1720753-2008-16303
Event typeMalfunction
Product problemY
Date received2008-02-21
Report sourceHealth Professional, User facility
NarrativeIT WAS REPORTED THAT THE 9800 SYSTEM WAS UNABLE TO RECALL IMAGES FROM THE IMAGE DIRECTORY. ALSO THERE WAS A COMMUNICATION FAILURE WITH THE KEYBOARD. THE SYSTEM WAS REBOOTED SEVERAL TIMES BEFORE THE IMAGES COULD BE RETRIEVED. NO PATIENT INJURY WAS REPORTED.
SourceopenFDA MAUDE (device adverse events)

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