Philips North America, LLC recalls HeartStart XL+ Defibrillator/Monitor, Model 861290
Recalled Product
HeartStart XL+ Defibrillator/Monitor, Model 861290
Hazard / Issue
The rotary therapy selector switch may fail, resulting in unexpected device behavior. These behaviors include: The device may not turn on; The device may not perform the selected function; The device may deliver a shock with an energy level different from the setting selected by the user.
Issued by
FDA
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