The air/water/instrument channel connector of the oer-3 was returned to olympus medical systems corp.(omsc) for evaluation.Omsc confirmed that the air/water/instrument channel connector was broken.Device history record review indicates that the product was manufactured and tested in accordance with all applicable procedures and met all final product release criteria.The exact cause was unknown; however, the following was supposed to be the cause.The user repeatedly applied a rotational force to the connector of the reprocessing basin of the device.
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