Model Number R SERIES |
Device Problem
Device Displays Incorrect Message (2591)
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Patient Problem
No Information (3190)
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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 while attempting to treat a patient (age & gender unknown), the device displayed a "pacer warning 124" message.Complainant did not indicate that there was any adverse effect to the patient due to the reported malfunction.
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Manufacturer Narrative
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This report was inadvertently submitted as a duplicate.The reported event was originally reported under medwatch 1220908-2018-01204 for the second device used on the same patient event.Analysis of reports of this type has not identified an increase in trend.
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Search Alerts/Recalls
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