Model Number 8011-0501-01 |
Device Problem
Failure to Discharge (1169)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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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 associated defibrillator failed to discharge using these internal handles.Complainant indicated that there was no patient involvement in the reported malfunction.
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Manufacturer Narrative
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Zoll medical corporation evaluated the internal handles and the customer's report was not replicated or confirmed.The handles used with a test r series and spoons were put through extensive testing including shock testing and continuity testing without duplicating the report.The internal handles were scrapped as a precaution.A replacement set was sent to the customer.No trend is associated with reports of this type.
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Search Alerts/Recalls
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