Model Number E SERIES |
Device Problem
Improper Alarm (2951)
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Patient Problem
No Patient Involvement (2645)
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Event Type
malfunction
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Manufacturer Narrative
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Zoll medical corporation has not received the device for evaluation and this complaint is still under investigation.
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Event Description
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Complainant alleged that during a routine shift check by a clinician, the device displayed a "cable fault" message.Complainant indicated that there was no patient involvement in the reported malfunction.
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Manufacturer Narrative
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The device was not returned to zoll medical (b)(4); the device's multi-function cable was removed and returned.The multi-function cable was put through extensive testing without duplicating the malfunction.The cable was scrapped.Analysis for reports of this type has not identified an increase in trend.
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Search Alerts/Recalls
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