Model Number R SERIES |
Device Problems
Mechanics Altered (2984); Activation Problem (4042)
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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 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 powers up in the incorrect mode and did not respond to the front panel controls.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; the customer's report was observed and attributed to a system interconnection flex cable that was not properly seated.The cable was reseated to correct the report.Analysis for reports of this type has not identified an increase in trend.
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Search Alerts/Recalls
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