This report is being supplemented to provide additional information based on 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, the root cause could not be determined.It is likely the reported event occurred due to stress from repeated use, external factors, or handling.The event can be detected by handling the device in accordance with the following ifu: 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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