The device was returned to zoll medical corporation for evaluation.The customer's report was not confirmed or replicated.The device was put through extensive testing including daily/weekly/monthly self-test and stress testing without duplicating the report.An internal inspection of the device found no discrepancies.The device was sent to the inventory and a replacement device was sent to the customer.The pads were not returned for evaluation.Analysis of reports of this type has not identified an increase in trend.
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