Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290 The HeartStart XL+ Recalled by Philips Healthcare Inc. Due to Philips HeartStart XL+ Defibrillator/Monitor may become locked out...
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 Healthcare Inc. directly.
Affected Products
Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290 The HeartStart XL+ is intended for use in a hospital setting by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced life support or defibrillation
Quantity: 3785 units
Why Was This Recalled?
Philips HeartStart XL+ Defibrillator/Monitor may become locked out of clinical use
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips Healthcare Inc.
Philips Healthcare Inc. has 36 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report