Model Number MSERIES |
Device Problem
Failure to Deliver Shock/Stimulation (1133)
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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 functional testing, the device failed to discharge using external paddles.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 not returned to zoll medical corporation; the device's paddles were returned.The customer's report was duplicated and attributed to a faulty button spring for the shock button on the paddles.The customer received a set of replacement paddles.Analysis for reports of this type has not identified an increase in trend.
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Manufacturer Narrative
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The device was returned to zoll medical (b)(4); the customer's report was duplicated and attributed to the external paddle set.A replacement paddle set was sent 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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