Reported Jun 24, 2020 · Terminated
DDU-2400EN Lifeline PRO, UDI 00815098020270 - Product Usage: Automated External Defibrillators (AED) are indicated for…
Defibtech, LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Defibtech, LLC · 741 Boston Post Rd · Guilford, CT · 06437-2714
Is this the product you have?
- DDU-2400EN Lifeline PRO
- UDI 00815098020270 - Product UsageAutomated External Defibrillators (AED) are indicated for use on victims
- of sudden cardiac arrest (SCA) who are- unconscious and unresponsive, not breathing or not breathing normally
- Lot codes and dates
- Serial Number 400101322
- Amount recalled
- 860
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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