This supplemental medwatch report is reporting the evaluation of the device and correcting information submitted on the initial medwatch report.Please reference section b3.Device evaluation: zoll medical corporation evaluated the device and the customer's report was not replicated or confirmed.The device was put through extensive testing including functional testing, defib/pacer stress testing, bench handling, and defib cycling without duplicating the report.The electrodes used were not returned as part of this investigation.Review of the clinical file showed a successful defibrillation.The user then turned the on the pacer mode.The device went to p3 lead and captured pacing, however, after some time, there was artifact on the leads, but the pacer function was still active and capturing.There was no error recorded in the logs during pacing.No trend is associated with reports of this type.
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