Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips HeartStart FRx AED. Recalled by Philips Electronics North America Corp. Due to An issue with one of the electric components...
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 Electronics North America Corp. directly.
Affected Products
Philips HeartStart FRx AED.
Quantity: Total for FRx and HS1 - 660,519 defibrillators
Why Was This Recalled?
An issue with one of the electric components (a resistor) could result in the device not delivering a shock when needed.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips Electronics North America Corp.
Philips Electronics North America Corp. has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report