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Cardiac Science Recalls
2 recalls on record · March 2, 2016 to July 10, 2019 · Medical Devices
Recalls by year
16
19
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 10, 2019Medical DevicesFDA
Cardiac Science Corporation recalls Powerheart¿ G5 Automatic AED
Hazard: Sub-supplier s documentation for specific Printed Circuit Boards (PCB) is insufficient to determine if the devices conform to specifications.
March 2, 2016Medical DevicesFDA
Cardiac Science Corporation recalls 9131-001 Defibrillation Electrodes, Lot No. 141125-02 Used in Powerheart G3 9300A, 9300E, 9300P, 9390A, and 9390E AEDs
Hazard: Defibrillation electrodes may increase electrical impedance over time. If impedance becomes too high, the AED will fail the electrode self-test and it will not be Rescue Ready, the AED STATUS INDICATOR will be RED and the AED will beep. This is normal behavior when the impedance limit is exceeded. The high impedance electrodes require replacement.