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 03/26/2023 |
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 while attempting to cardiovert a patient (age & gender unknown), the device would not sync to the patient's heart rhythm.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 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 synchronized cardioversion testing, using known good test accessories without duplicating the report.The device was recertified and returned to the customer.The reported problem was unable to be confirmed from the logs review.No trend is associated with reports of this type.
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Search Alerts/Recalls
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