This supplemental report is being submitted to provide the results of the legal manufacturer's final investigation.A review of the device history record found no deviations that could have caused or contributed to the reported issue.Based on the results of the investigation, a definitive root cause could not be determined.However, it is likely that the suggested event occured due to stress of repeated use, external factors, or handling.The event can be prevented/detected by following the instructions for use described in manual ¿chapter 3 preparation and inspection 3.2 preparation and inspection of the endoscope".Olympus will continue to monitor field performance for this device.
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