Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
The LIFEPAK 1000 defibrillator is intended for use by personnel Recalled by Physio-Control, Inc. Due to The firm has received complaints that the LIFEPAK...
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 1000 defibrillator is intended for use by personnel who are authorized by a physician/medical director and are trained in CPR and the use of the LIFEPAK 1000 defibrillator.
Quantity: total 133,330 units (50,046 units in the US)
Why Was This Recalled?
The firm has received complaints that the LIFEPAK 1000 Defibrillator is unexpectedly powering off during device usage.
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