Defibtech recalls DDU-2450 Lifeline AEDs with specific model numbers and serials due to risk of failing to deliver shock during cardiac arrest emergencies.
A component issue may cause the AED to abort a shock delivery or reset unexpectedly, which may cause an affected device to fail to delivery shock, and/or to fail to deliver shock in range.
Defibtech is recalling certain DDU-2450 Lifeline AEDs that may fail to deliver shock during cardiac arrest emergencies. This could be life-threatening if used when someone needs defibrillation.
The AEDs may abort shock delivery or reset unexpectedly, causing them to fail to shock a person in cardiac arrest. This could be fatal if the device doesn't work when needed.
People with Defibtech DDU-2450 Lifeline AEDs matching the listed model numbers or serials are affected. Those who use these devices in cardiac emergencies are at highest risk.
Check for model numbers DDU-A2450EN, DDU-E2450DE, DDU-E2450EN, DDU-E2450FR, or DDU-E2450TH. Also check the serial numbers listed in the recall notice.
Identify your AED's model number and serial number to confirm if it's in the recall list.
Reach out to Defibtech directly for guidance on next steps if your device is affected.
The AEDs may fail to deliver shock during cardiac arrest emergencies due to a component issue.
Check for model numbers DDU-A2450EN, DDU-E2450DE, DDU-E2450EN, DDU-E2450FR, or DDU-E2450TH, or the listed serial numbers.
Contact Defibtech directly for guidance on next steps if your device is affected.
We’ve drafted a message you can send Defibtech to request your refund or repair — edit it as you like.
Subject: Recall Z-2394-2020 — Defibtech Defibtech Hello, I own a Defibtech that is covered by recall Z-2394-2020 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.