Stryker Lifepak 15 Monitor/Defibrillator Recall [US]

US FlagUS/Silver Spring: Stryker Lifepak 15 Monitor/Defibrillator Recall [US]Stryker, a Kalamazoo, Michigan establishment, recalls an estimated 13,003 Lifepak 15 Monitor/Defibrillator Medical Devices due to suspected operational malfunction and consequential risk of device lock-up after a defibrillation shock is delivered and subsequent failure to function, possibly leading to delay or complete failure of the device to operate in an emergency and possible injury and/or death, all serious health and safety hazards. Deaths reported.

FDA: http://ht.ly/1P0530nAsHs

Direct link: https://www.fda.gov/Safety/Recalls/ucm630455.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Monitor/Defibrillator Medical Devices are subject to this recall:

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