Model Number 8011-0501-02 |
Device Problem
Output Problem (3005)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Type
malfunction
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Event Description
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Complainant alleged that during biomed testing, the associated defibrillator's defib output was out of specification 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 has not received the device for evaluation and this complaint is still under investigation.
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Manufacturer Narrative
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The complainant was contacted for return of the device.The device has not been returned to zoll for evaluation.
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Search Alerts/Recalls
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