Reported Apr 5, 2023 · Ongoing
DDU-100 Lifeline Automated External Defibrillator (AED)-Indicated for use on victims of sudden cardiac arrest
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-100 Lifeline Automated External Defibrillator (AED)-Indicated for use on victims of sudden cardiac arrest
- Lot codes and dates
- UDI-DI00815098020003
- Serial Numbers
101702198101702263101702424101702524101702535101702540101702544101702545101703267101703269101703272101703274101703276101703277101703278101703281101703312101703326101703378101703407101703411101703412101703419101703424101703427101703464101703465101703600101704106
- Amount recalled
- 29 units
Where it was sold
- Nationwide
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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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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