This device was returned for service; however, did not meet manufacturing specifications during pre-repair assessment.Reliability engineering evaluated the device and the reported condition was confirmed.The assignable root cause was determined to be due to wear from normal use over time.If additional information should become available, a supplemental medwatch report will be submitted accordingly.
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It was reported by switzerland that during service and evaluation, it was discovered that there was damaged component- cable/cord/wiring on the motor device.It was noted in the service order that the motorflex was defective, the engine was worn out and there was a hole in the hose.It was further determined that there was heat.This event did not occur during surgery.There was no patient involvement.There were no reports of injuries, medical intervention or prolonged hospitalization.The exact date of this event was unknown.All available information has been disclosed.If additional information should become available, a supplemental medwatch report will be submitted accordingly.
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