Model Number AED PLUS |
Device Problem
Incorrect Interpretation of Signal (1543)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 09/28/2023 |
Event Type
malfunction
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Manufacturer Narrative
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Zoll medical corporation has not received the product 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 monitor a 27-year-old female patient, the device issued a "shock advised" prompt for a heart rhythm they believe was non-shockable.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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The device was not returned to zoll medical corporation for evaluation.Instead, the customer indicated the device was connected to an alert and orientated patient.The aed plus operator's guide states "do not use when a patient: is conscious; or is breathing; or has a detectable pulse or other signs of circulation." analysis of reports of this type has not identified an increase in trend.
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Search Alerts/Recalls
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