Model Number X SERIES |
Device Problem
Electrical Shorting (2926)
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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 received the product and will be providing a supplemental report when our investigation is completed.
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Event Description
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Complainant alleged that during a routine shift check by a clinician, the device displayed a "short detected" message.Complainant indicated that there was no patient involvement in the reported malfunction.
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Manufacturer Narrative
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The device was returned to zoll medical corporation for evaluation.The customer's report was not replicated or confirmed.The device was put through extensive testing including defib shock testing and impedance testing without duplicating the report.An internal inspection of the device found no discrepancies.Review of the device log found no evidence of the report.The device was recertified and returned to the customer.No trend is associated with reports of this type.
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Search Alerts/Recalls
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