Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Zoll Medical X Series Recalled by ZOLL Medical Corporation Due to Defibrillator/Pacemaker/Monitor May Latch in a Continuous Device Reset...
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 ZOLL Medical Corporation directly.
Affected Products
Zoll Medical X Series, PropaqMD, PropaqM Defibrillator/Pacemaker/Monitor With System Software Version 02.10.02.00 or Higher, automated external defibrillator.
Quantity: 3,169 units
Why Was This Recalled?
Defibrillator/Pacemaker/Monitor May Latch in a Continuous Device Reset Loop and cannot be used
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About ZOLL Medical Corporation
ZOLL Medical Corporation has 14 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report