Model Number AED PLUS |
Device Problem
Incorrect Interpretation of Signal (1543)
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Patient Problem
Necrosis (1971)
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Event Date 04/01/2023 |
Event Type
Death
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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 defibrillate an 84-year-old male patient, the device gave a "no shock advised" prompt for a rhythm clinicians believed was shockable.Complainant indicated that the clinician obtained another device to continue treating the patient.Complainant indicated that the patient subsequently expired.
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Manufacturer Narrative
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The customer was contacted for return of the suspect product.The customer has responded and indicated they were able to view the ecg and the device is working properly.Therefore, the product will not be returning to zoll.
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Search Alerts/Recalls
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