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, the device failed to discharge.Complainant indicated that there was no patient involvement in the reported malfunction.
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Manufacturer Narrative
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The complainant was contacted for return of the device.The customer has responded that the handles have been disposed and indicated the handles will not be returning to zoll for evaluation.
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Search Alerts/Recalls
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