Model Number R SERIES |
Device Problem
Pacing Problem (1439)
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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 device was unable to pace.Complainant indicated that there was no patient involvement in the reported malfunction.
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Manufacturer Narrative
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The customer was contacted for return of the suspect product.The product has not been returned to zoll for evaluation.
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Manufacturer Narrative
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The device was returned to zoll medical corporation.The customer's report was duplicated and attributed to a faulty relay on the pace/defib engine.The pace/defib engine 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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