The customer's report was observed during review of the device's history log.The device was put through extensive testing which included bench handling, power cycling, and ecg monitoring functional stress testing without duplicating a device malfunction.The defib cable receptacle and the monitor board were replaced as a precaution.The device was recertified and returned to the customer.The customer also received a new multifunction cable and was asked to discard the older one not returned.Analysis for reports of this type has not identified an increase in trend.
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