The device was returned to zoll medical corporation for evaluation.The customer's report was not replicated or confirmed.The device was put through extensive testing including bench handling, discharging, and defib cycling without duplicating the report.An internal inspection of the device found no discrepancies.The device log does not capture reports of this nature.The customer's power related accessories were not returned for evaluation.The device was recertified and returned to the customer.No trend is associated with reports of this type.
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