The device was returned to zoll medical corporation.The customer's report was not replicated or confirmed.The device passed all testing including discharging, bench handling, multifunction continuity testing, and defib cycling without duplicating the report.Review of the device logs did not identify any failures of indication that there was a problem using defib electrodes and the multifunction cable.The device was recertified and returned to the customer.It's important to mentioned that the customer's accessory ecg cable was determined to be faulty and replaced.Analysis of reports of this type has not identified an increase in trend.
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