Model Number 1001-001150-01 |
Device Problem
Failure to Deliver Shock/Stimulation (1133)
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Patient Problem
Insufficient Information (4580)
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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 associated device failed to discharge using these paddles.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 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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