Model Number X SERIES |
Device Problem
Failure of Device to Self-Test (2937)
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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 device failed self-test for defib and pacer functions.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 customer's report was duplicated at zoll canada and the processor/bridge/pace board was replaced to remedy the report.The device was recertified and returned to the customer.Analysis of reports of this type has not identified an increase in trend.
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Search Alerts/Recalls
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