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 Device may fail to turn on or unexpectedly...
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: 24,738 units
Why Was This Recalled?
Device may fail to turn on or unexpectedly attempt to restart, rendering it unable to return to a ready for use state. Additionally, this issue may occur when the device is in standby mode, when attempting to power on to run a self-test. If this occurs, the device will indicate that it is not ready for use.
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