FDA Update: LIFEPAK 15 Monitor/Defibrillators Recalled Due to Shock Failure – American College of Cardiology

On Jan. 10, B. Stryker initiated a voluntary recall of specific units of their LIFEPAK 15 monitor/defibrillators due to an issue that may cause these devices to fail to deliver a defibrillation shock after the “shock” button on the keypad is pressed. Stryker is contacting customers with impacted devices to schedule the correction of their device(s), which will include…

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