Defibtech recalls DDU-100 AEDs with specific serial numbers due to untested components that may fail during cardiac arrest emergencies.
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.
Defibtech is recalling certain DDU-100 AEDs because a component in the device wasn't properly tested and could fail to deliver life-saving shocks during cardiac arrest. This is serious because sudden cardiac arrest requires immediate defibrillation to save lives.
The AEDs contain a component that wasn't tested for durability and reliability. If this component malfunctions, the device might not deliver the necessary shock to stop cardiac arrest, which could be fatal.
Anyone who owns or uses the recalled DDU-100 AEDs with the listed serial numbers. Emergency responders and individuals with cardiac arrest training are most at risk if the device fails during a critical event.
Check the serial number on your DDU-100 AED. The affected units have specific serial numbers listed in the recall notice, including 101702198 through 101704106.
Look for the serial number on your DDU-100 AED to see if it matches the list of affected units provided in the recall.
The AEDs contain a component that wasn't tested for durability and reliability, which could cause the device to fail during cardiac arrest emergencies.
Check the serial number on your AED to confirm if it's affected. If it is, contact Defibtech for further instructions.
The recall states the device could fail to deliver therapy during cardiac arrest, which could be fatal. However, the remedy does not specify immediate action to stop use.
We’ve drafted a message you can send Defibtech to request your refund or repair — edit it as you like.
Subject: Recall Z-1312-2023 — Defibtech Defibtech Hello, I own a Defibtech that is covered by recall Z-1312-2023 from Defibtech. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
