Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
The LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators. Product part's Recalled by Physio Control, Inc. Due to LIFEPAK CR Plus or LIFEPAK Express Automated External...
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
The LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators. Product part's numbers: 3200731-xxx, 3202177-xxx, U3200731-xxx, and U3202177-006. Automated external defibrillators.
Quantity: 54,197 units in US and 78,627 units internationally (total 132, 824 units)
Why Was This Recalled?
LIFEPAK CR Plus or LIFEPAK Express Automated External Defibrillators (AEDs) are recalled due to the potential to experience an early internal battery depletion issue.
Where Was This Sold?
Worldwide Distribution.
About Physio Control, Inc.
Physio Control, Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report