Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DDU-100 Lifeline Automated External Defibrillator (AED)-Indicated for use on victims Recalled by Defibtech, LLC Due to A component of a sub-assembly used in 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 Defibtech, LLC directly.
Affected Products
DDU-100 Lifeline Automated External Defibrillator (AED)-Indicated for use on victims of sudden cardiac arrest
Quantity: 29 units
Why Was This Recalled?
A component of a sub-assembly used in the affected AEDs had not undergone durability and reliability testing, and if a malfunction occurs, therefore the device could fail to deliver therapy.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Defibtech, LLC
Defibtech, LLC has 14 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report