Model Number R SERIES |
Device Problem
Pacing Problem (1439)
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Patient Problem
No Information (3190)
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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 while attempting to treat a patient (age & gender unknown) the device stopped pacing the patient.Complainant did not indicate that there was any adverse effect to the patient due to the reported malfunction.
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Manufacturer Narrative
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Zoll medical corporation evaluated the device and the reported malfunction was not replicated or confirmed.The device was put through extensive testing without duplicating the malfunction.Review of the device logs did not show any pacer related failure messages.The device was recertified and returned to the customer.The associated electrode pads were not available for evaluation.Analysis for reports of this type has not identified an increase in trend.
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Search Alerts/Recalls
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