Zoll medical corporation evaluated the device and the customer's report was not replicated or confirmed.The device was put through extensive testing which included stress testing, pacer testing using a stimulator, keypad testing, bench handling, defib testing, and ecg testing without duplicating any device malfunction.The multifunction cable, electrode pads or cpr adapter were not returned as part of the investigation.Review of the logs found evidence of pacing difficulties.However, the logs do not confirm a device malfunction.The device was recertified and returned to the customer.No trend is associated with reports of this type.
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