Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received Recalled by Physio-Control, Inc. Due to Monitor/Defibrillator may not deliver a shock after the...
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
LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an affected keypad.
Quantity: 29952
Why Was This Recalled?
Monitor/Defibrillator may not deliver a shock after the "Shock" button on the keypad is pressed as a result of oxidation that has formed over time within the button.
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