Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PHYSIO CONTROL LIFEPAK CR2 Defibrillator 3321605-xxx The LIFEPAK CR2 defibrillator Recalled by Physio-Control, Inc. Due to Due to complaints received regarding missing lid magnets...
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 Physio-Control, Inc. directly.
Affected Products
PHYSIO CONTROL LIFEPAK CR2 Defibrillator 3321605-xxx The LIFEPAK CR2 defibrillator is designed for indoor and outdoor use in a stationary environment. After the electrode pads are applied, the fully automatic model evaluates the heart rhythm and, if a shockable rhythm is detected, delivers a shock without any responder assistance. The LIFEPAK CR2 defibrillator is indicated for use on patients 1 year of age or older in cardiopulmonary arrest.
Quantity: 89,763 units
Why Was This Recalled?
Due to complaints received regarding missing lid magnets which may result in premature battery depletion.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Physio-Control, Inc.
Physio-Control, Inc. has 38 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report