Product Wiki · Recalls · Health Canada — Medical Devices

ZOLL AED Pro External Defibillator (2019-06-11) — recall 59180

Health Canada — Medical Devices · Canada · 2019-06-18 · Type I

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Agency
Health Canada — Medical Devices
Recall identifier
59180
Date of alert
2019-06-18
Country / jurisdiction
Canada
Risk level
Type I
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: A field report was received of the AED Pro prompting "unit failed" during a defibrillation shock attempt. Investigation traced the problem to an area of an internal circuit board that is susceptible to isolation breakdown. If the isolation breakdown occurs during a shock attempt, the device will issue the "unit failed" message and prevent delivery of the energy to the patient.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/zoll-aed-pro-external-defibill

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