This report for non-fatal serious injury/device malfunction has been stored under the covid-19 pandemic in accordance with the guidance published by fda, postmarketing adverse event reporting for medical products and dietary supplements during a pandemic.The device was not returned to olympus medical systems corp.(omsc), therefore omsc cannot investigate the device.The instruction manual provides the correct reprocess procedure of the device.Omsc concluded that this phenomenon is attributed to the inappropriate handling by the user.If additional information becomes available, this report will be supplemented.
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