Model Number R SERIES |
Device Problem
Unable to Obtain Readings (1516)
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Patient Problem
Injection Site Reaction (4562)
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Event Type
malfunction
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Event Description
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Complainant alleged that during a biomed testing, the device displayed a "check pads" message.Complainant indicated that there was no patient involvement in the reported 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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Manufacturer Narrative
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The device was returned to zoll medical corporation for evaluation.The customer's report was observed during review of the device activity log.However, the device was put through extensive testing including functionality testing without duplicating the report.Internal inspection of the device found no discrepancies.The device was recertified and returned to the customer.Analysis for reports of this type has not identified an increase in trend.
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Search Alerts/Recalls
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