Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
HeartStart XL+ Defibrillator/Monitor Recalled by Philips North America, LLC Due to The rotary therapy selector switch may fail, resulting...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Philips North America, LLC directly.
Affected Products
HeartStart XL+ Defibrillator/Monitor, Model 861290
Quantity: 23,749 Units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips North America, LLC
Philips North America, LLC has 88 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report