Model Number R SERIES |
Device Problem
Sparking (2595)
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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, a spark was seen from the device's multifunction cable.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 device was returned to zoll medical uk service department; the customer's report was not replicated or confirmed.The device was put through extensive testing without duplicating the report.An internal inspection found no discrepancies.Accessories were tested with no problem found.The training pads were scrapped as a precaution.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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