Model Number 8011-0501-01 |
Device Problem
Failure to Deliver Shock/Stimulation (1133)
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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 functional testing, these internal handles failed to discharge.Complainant did not indicate that there was any patient involvement in the reported malfunction.
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Manufacturer Narrative
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The internal handles were returned to zoll medical corporation and the customer's report was not replicated or confirmed.The internal handles passed testing and were able to discharge at all energy levels with no faults found.The internal handles were forwarded to scrap as a precaution.Analysis of reports of this type has not identified an increase in trend.
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Search Alerts/Recalls
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