Defibtech recalls DDU-2300 Lifeline/ReviveR View AEDs with specific model numbers and serial ranges due to risk of failing to deliver shock during cardiac 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-2300 Lifeline/ReviveR View AEDs because a component issue may cause the device to fail to deliver shock during cardiac emergencies. This could be life-threatening if used when needed.
A component issue in the device may cause it to abort shock delivery or reset unexpectedly, which could prevent the AED from delivering a shock when needed during a sudden cardiac arrest event.
People who own or use Defibtech DDU-2300 Lifeline/ReviveR View AEDs with the listed model numbers and serial ranges are affected. Emergency responders and individuals with cardiac arrest training are most at risk.
Check for model numbers DDU-C2300EN, DDU-C2300CA, DDU-A2300EN, or DDU-E2300EN. Also look for the specific serial numbers listed in the recall notice.
Verify your AED's model number against the listed DDU-C2300EN, DDU-C2300CA, DDU-A2300EN, or DDU-E2300EN.
Confirm your AED's serial number is within the provided range of numbers listed in the recall notice.
The recall is due to a component issue that may cause the AED to fail to deliver shock during cardiac emergencies, which could be life-threatening.
Check your AED's model number and serial number against the listed numbers in the recall notice to determine if it's affected.
The recall record does not specify a remedy or fix for this issue.
We’ve drafted a message you can send Defibtech to request your refund or repair — edit it as you like.
Subject: Recall Z-2392-2020 — Defibtech Defibtech Hello, I own a Defibtech that is covered by recall Z-2392-2020 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.
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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.
