The device was returned to zoll medical corporation for evaluation.The customer's report was observed during review of the device data logs.However, the device was put through extensive testing including bench testing and ecg stressing without duplicating the report.The multi function cable was not returned and could not be visually inspected or functionally tested.The defib receptacle was replaced as a precaution.A new multi function cable was sent to the customer.The customer was instructed to discard the multi function cable that was used with the device.The device was recertified and returned to the customer.Analysis of reports of this type has not identified an increase in trend.
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