Zoll medical corporation evaluated the device and the reported malfunction was not replicated or confirmed.The device was put through extensive testing without duplicating the malfunction.The device history log shows evidence of a connectivity issue between the electrode pads and the patient, however, this does not necessarily indicate a device malfunction.The event electrodes were not returned to zoll for evaluation as part of this investigation.The device was recertified and returned to the customer.No trend is associated with reports of this type.
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