Lifeline Pro DDU-E2400Recalls & reported problems
Defibtech, L.L.C. · Class 3
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00815098020270), received between Jan 28, 2026 and Jun 25, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Premature Discharge of Battery” (2 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Premature Discharge of Battery2
- Battery Problem1
- Electrical /Electronic Property Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 25, 2026Electrical /Electronic Property Problem
AN INTERNATIONAL DISTRIBUTOR REPORTED THAT THEIR CUSTOMER'S AED ASI IS FLASHING RED, AND THE DEVICE IS REPORTING A SERVICE CODE. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25631126 ↗MalfunctionFeb 20, 2026Premature Discharge of Battery
A CUSTOMER REPORTED THAT THEIR AED WOULD NOT POWER ON AND THEY COULD NOT REMOVE THE BATTERY. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24405463 ↗MalfunctionFeb 19, 2026Premature Discharge of Battery
AN INTERNATIONAL DISTRIBUTOR REPORTED THEIR CUSTOMER'S AED WOULD NOT POWER ON, BUT IT POWERED ON WITH A SPARE BATTERY. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24392805 ↗MalfunctionJan 28, 2026Battery Problem
THE DISTRIBUTOR REPORTED THAT THEIR CUSTOMER REPORTED THE AED'S BATTERY PACK WAS UNABLE TO POWER IT ON. THE BATTERY THAT WAS IN THE AED HAS AN EXPIRATION OF 03/31/2028. ANOTHER BATTERY PACK WAS INSERTED AND THE AED WORKED AS DESIGNED. NO ADDITIONAL INFORMATION PROVIDED. THIS REPORTED EVENT DID NOT OCCUR DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24198619 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.