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, and although we could not specify the root cause of the suggested event, it is likely that the defect was caused by the following: the image sensor unit cable had shorted out since the universal cord was kinked, and the circuit board had a defect since the video connector was dented.The suggested event can be detected by handling the device in accordance with the instructions for use (ifu): chapter 3 preparation and inspection, 3.8 inspection of the endoscopic system olympus will continue to monitor field performance for this device.
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