Defibtech recalls DDU-2400EN Lifeline PRO AEDs with UDI 00815098020270 due to risk of failing to deliver shock during cardiac arrest emergencies. Affected units may not function properly when needed.
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 its DDU-2400EN Lifeline PRO AEDs with specific serial numbers because they might fail to deliver shock during cardiac arrest emergencies. This could be dangerous if someone needs defibrillation but the device doesn't work properly.
The AED may stop delivering shocks or reset unexpectedly during use, which could cause it to fail when needed for sudden cardiac arrest. This means the device might not work properly when someone is in immediate danger.
People who own or use Defibtech DDU-2400EN Lifeline PRO AEDs with the serial number 400101322 are affected. Those who rely on these devices for cardiac emergencies are at the highest risk.
Check your AED's serial number. The affected units have the serial number 400101322 and the unique identifier (UDI) 00815098020270.
Look for the serial number 400101322 on your DDU-2400EN Lifeline PRO AED.
The AED may stop delivering shocks or reset unexpectedly during use, which could cause it to fail when needed for sudden cardiac arrest.
Check your AED's serial number. If it's 400101322, contact Defibtech for guidance.
The recall record does not mention a remedy or fix.
We’ve drafted a message you can send Defibtech to request your refund or repair — edit it as you like.
Subject: Recall Z-2393-2020 — Defibtech Defibtech Hello, I own a Defibtech that is covered by recall Z-2393-2020 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.
