Model Number MSERIES |
Device Problem
Device Operates Differently Than Expected (2913)
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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 received the product and will be providing a follow-up 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 was unable to obtain an ecg signal.Complainant indicated that there was no patient involvement in the reported malfunction.
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Manufacturer Narrative
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This follow up medwatch report is reporting the evaluation of the device.This follow up medwatch report is also correcting information submitted on the initial medwatch report.The device was returned to zoll medical corporation; the malfunction was duplicated and the device's el display was replaced to remedy the problem.Analysis for reports of this type has not identified an increase in trend.
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Event Description
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Complainant alleged that during a routine shift check by a clinician, the device's display was missing information.Complainant indicated that there was no patient involvement in the reported malfunction.
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Search Alerts/Recalls
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