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Stryker Launches Voluntary Field Action for Specific Units of the LIFEPAK® 15...

Discussion in 'FDA Recalls' started by Food and Drug, Feb 1, 2019.

  1. The company is notifying certain LIFEPAK 15 customers of an issue that may cause the device to lock up after a defibrillation shock is delivered. The lock-up condition is defined as a blank monitor display with LED lights on, indicating power to the device, but no response in the keypad and device functions. A device in this condition has the potential to delay delivery of therapy, and this delay in therapy has the potential to result in serious injury or death.

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  2. Medic man

    Medic man Puppy

    Fortunately our new 15s were manufactured after they found and fixed this. I would hate to be on a cardiac arrest and have my monitor/defibrillator crash.
     

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