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 Recalled by Philips Medical Systems, Inc. Due to A component on the HeartStart XL+ Therapy Board...
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 Medical Systems, Inc. directly.
Affected Products
Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290, automatic external defibrillator.
Quantity: 19 units
Why Was This Recalled?
A component on the HeartStart XL+ Therapy Board could malfunction potentially affecting the ability to deliver therapy
Where Was This Sold?
This product was distributed to 2 states: IN, WA
About Philips Medical Systems, Inc.
Philips Medical Systems, Inc. has 65 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report