Model Number X SERIES |
Device Problem
Unable to Obtain Readings (1516)
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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 biomed testing, the device was unable to obtain an ecg signal via attached electrode pads.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 (b)(4) for evaluation.The reported malfunction was observed and attributed to the defib cable receptacle.The defib harness, defib receptacle was replaced to resolve the malfunction.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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