Model Number R SERIES |
Device Problem
Device Displays Incorrect Message (2591)
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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 received the product and will be providing a follow-up report when our investigation is completed.
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Event Description
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Complainant alleged that during functional testing, the device displayed a "pacer fault " message.The complainant did not know what number pacer fault occurred.Complainant indicated that there was no patient involvement in the reported malfunction.
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Manufacturer Narrative
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The reported malfunction was observed and attributed to a faulty inductor on the pace/defib engine board.Analysis of reports of this type has not identified an increase in trend.
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Search Alerts/Recalls
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