Model Number R SERIES |
Device Problem
Mechanics Altered (2984)
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Patient Problem
No Patient Involvement (2645)
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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 a routine shift check by a clinician, the device was unable to switch modes.Complainant indicated that there was no patient involvement in the reported malfunction.
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Manufacturer Narrative
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The customer's report was observed at zoll medical corporation; during disassembly of the device to determine root cause, the technician observed damage consistent with mishandling.The system interconnect flex cables were reseated 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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