Model Number PROPAQ MD |
Device Problem
Failure to Power Up (1476)
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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 biomed testing, the device would not power up.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 not received the device for evaluation and this complaint is still under investigation.
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Manufacturer Narrative
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The device was returned to zoll medical singapore; the customer's report was duplicated and the monitor board was replaced to resolve the report.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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