Model Number E 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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Event Description
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Complainant alleged that during biomed testing, the device displayed a "defib fault 79" message.Complainant indicated that there was no pt involvement in the reported malfunction.
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Manufacturer Narrative
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Zoll medical corp has not rec'd the product for eval and this complaint is still under investigation.
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Manufacturer Narrative
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The device was returned to zoll medical canada.The malfunction was duplicated and attributed to a damaged flex cable on the system board.The flex cable was replaced to remedy the condition.Analysis for reports of this type has not identified an increase in trend.
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Search Alerts/Recalls
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