Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips Recalled by Philips North America LLC Due to Customers were not notified of previous recalls associated...
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
Philips, HeartStart FR2 + Defibrillator, Model # M3860A and M3861A
Quantity: 4 units
Why Was This Recalled?
Customers were not notified of previous recalls associated with various defibrillator models.
Where Was This Sold?
This product was distributed to 12 states: CA, CT, FL, GA, IN, MI, MO, NJ, NY, OH, TX, WA
About Philips North America LLC
Philips North America LLC has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report