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FDAOctober 16, 2019device

HeartStart XL+ Defibrillator/Monitor, Model 861290

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

philips north americaphilipsphilips north

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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