Model Number X SERIES |
Device Problem
Pacing Problem (1439)
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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 biomed testing, the device did not have pacer output.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 corporation for evaluation; instead a log file was provided.The reported malfunction was observed in the device's history logs.Zoll business partner indicated that the processor/bridge/pace board was replaced as a precaution.Analysis for reports of this type has not identified an increase in trend.
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Manufacturer Narrative
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The device was not returned to zoll medical corporation for evaluation.Instead the processor/bridge/pace board was returned to zoll medical corporation, united states.The customer's report was attributed to the processor/bridge/pace board.The board was scrapped.Analysis of reports of this type has not identified an increase in trend.
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Search Alerts/Recalls
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