Model Number X SERIES |
Device Problem
Inaccurate Synchronization (1609)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 12/30/2022 |
Event Type
malfunction
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Event Description
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Complainant alleged that while attempting to cardiovert a patient (age & gender unknown), the device's syncing process stopped when joules were being charged to deliver the shock.Complainant indicated that there was no adverse effect to the patient due to 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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Zoll medical corporation evaluated the device and the customer's report was not replicated or confirmed.The device was put through extensive testing including full functional testing and synchronization testing without duplicating the report.The device was recertified and returned to the customer.Review of the device activity logs did not show any faults that could be associated with customer report.No trend is associated with reports of this type.
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Search Alerts/Recalls
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