Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
LIFEPAK(R) defibrillation electrodes Recalled by Physio-Control, Inc. Due to The infant artwork on the product instructs incorrect...
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(R) defibrillation electrodes, Catalog # 11101-000016, MIN #3202380-006 The defibrillation electrodes are used only with LIFEPAK EXPRESS(R) AED, LIFEPAK CR(R) Plus AED, LIFEPAK 1000 defibrillator, or LIFEPAK 500 Biphasic AED s with a pink connector.
Quantity: 14,219 units in total
Why Was This Recalled?
The infant artwork on the product instructs incorrect pad placement. Also, the artwork is missing the Type BF Patient connection and High Voltage Warning symbols.
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