Model Number PROPAQ MD |
Device Problem
Failure of Device to Self-Test (2937)
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Patient Problem
Premature Labor (2465)
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Event Type
malfunction
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Manufacturer Narrative
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Additional procode = dro.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 failed self test for defib and pacer function.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.During disassembly of the device to determine root cause, the technician observed extensive impact damage consistent with mis-handling.Root cause could not be firmly established due to the observed damage.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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