Device evaluation of monitor sn (b)(4) has been completed.The reported problem (check te pad messages) has been confirmed.Upon investigation the monitor was unable to recognize an ecg or therapy electrode signal.The monitor's electrode belt connector had an intermittent connection, causing the reported messages.The monitor's enclosure showed evidence of physical abuse at the electrode belt connector.The root cause for the damaged connector was excessive force.No adverse event resulted from the defective monitor.
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