Lifeline View Configuration DDU-A2300Recalls & reported problems
Defibtech, L.L.C. · Class 3
All models of Lifeline View Configuration (2)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This Defibtech Lifeline View automated external defibrillator is a portable device that delivers a shock to a heart that has stopped. Many of the 114 reports describe batteries draining early, the unit failing to power on, or a flashing red light with a service code, and most note these problems did not occur during patient use. There are no deaths and no injuries. Reports fell to 22 in the last 12 months from 63 in the previous 12 months. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 114
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 114 adverse event reports that list this exact device (DI 10815098020208), received between Jun 20, 2019 and Jan 23, 2026 — classified as 114 malfunctions.
The most frequently reported specific device problem is “Premature Discharge of Battery” (49 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Premature Discharge of Battery49
- Failure to Power Up37
- Battery Problem9
- Failure to Deliver Shock/Stimulation8
- Display or Visual Feedback Problem2
- Failure to Sense2
- Incomplete or Inadequate Connection2
- No Audible Prompt/Feedback2
Patient problems
- No Clinical Signs, Symptoms or Conditions109
- Unspecified Heart Problem3
- Insufficient Information1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 25 most recent of 114 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 23, 2026No Audible Prompt/Feedback
A CUSTOMER REPORTED THEIR AED WILL NOT SPEAK. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24162035 ↗MalfunctionJan 23, 2026Premature Discharge of Battery
A CUSTOMER REPORTED THAT THEIR AED'S ASI IS FLASHING RED, AND REPORTING A SERVICE CODE. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24159834 ↗MalfunctionJan 12, 2026Premature Discharge of Battery
A CUSTOMER REPORTED A SERVICE CODE. ASI IS FLASHING RED. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24040770 ↗MalfunctionJan 12, 2026Premature Discharge of Battery
A CUSTOMER REPORTED A SERVICE CODE. ASI IS FLASHING RED. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24040749 ↗MalfunctionJan 5, 2026No Audible Prompt/Feedback
A CUSTOMER REPORTED THEIR AED WILL NOT SPEAK. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23963730 ↗MalfunctionDec 15, 2025Premature Discharge of Battery; Premature Discharge of Battery
A CUSTOMER REPORTED THAT THEIR AED'S ASI IS FLASHING RED, AND REPORTING A SERVICE CODE. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23802043 ↗MalfunctionDec 12, 2025Premature Discharge of Battery; Premature Discharge of Battery
A CUSTOMER REPORTED THAT THEIR AED'S ASI IS FLASHING RED, AND REPORTING A SERVICE CODE. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23790827 ↗MalfunctionDec 12, 2025Premature Discharge of Battery; Premature Discharge of Battery
A CUSTOMER REPORTED THAT UPON INSERTING A NEW BATTERY PACK, THEIR AED POWERED ON AND PROMPTED A SERVICE CODE. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23790826 ↗MalfunctionDec 5, 2025Premature Discharge of Battery; Premature Discharge of Battery
A CUSTOMER REPORTED THAT THEIR AED'S ASI IS FLASHING RED AND REPORTING A SERVICE CODE. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23728538 ↗MalfunctionDec 2, 2025Premature Discharge of Battery; Premature Discharge of Battery
A CUSTOMER REPORTED THAT THEIR AED'S ASI IS FLASHING RED, AND REPORTING A SERVICE CODE. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23696906 ↗MalfunctionDec 2, 2025Premature Discharge of Battery; Premature Discharge of Battery
A CUSTOMER REPORTED THAT THEIR AED'S ASI IS FLASHING RED, AND REPORTING A SERVICE CODE. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23696904 ↗MalfunctionDec 1, 2025Premature Discharge of Battery; Premature Discharge of Battery
A CUSTOMER REPORTED THAT THEIR AED'S ASI IS FLASHING RED, AND REPORTING A SERVICE CODE. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23682732 ↗MalfunctionNov 15, 2025Premature Discharge of Battery; Premature Discharge of Battery
A CUSTOMER REPORTED THAT THEIR AED'S ASI IS FLASHING RED, AND REPORTING A SERVICE CODE. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23564981 ↗MalfunctionNov 15, 2025Failure to Power Up; Failure to Power Up
A CUSTOMER REPORTED THAT THEIR AED'S ASI IS BLANK, AND THE AED WILL NOT POWER ON. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23564980 ↗MalfunctionNov 15, 2025Failure to Power Up; Failure to Power Up
A CUSTOMER REPORTED THAT THEIR AED'S ASI WAS FLASHING RED, AND THE AED WILL NOT POWER ON. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23564017 ↗MalfunctionNov 7, 2025Failure to Deliver Shock/Stimulation; Failure to Deliver Shock/Stimulation
A CUSTOMER REPORTED THAT THEIR AED'S ASI IS FLASHING RED, AND REPORTING A SERVICE CODE. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23501444 ↗MalfunctionNov 6, 2025Premature Discharge of Battery; Premature Discharge of Battery
A CUSTOMER REPORTED THAT UPON INSERTING A NEW BATTERY PACK, THEIR AED POWERED ON AND PROMPTED A SERVICE CODE. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23490984 ↗MalfunctionNov 6, 2025Premature Discharge of Battery; Premature Discharge of Battery
A CUSTOMER REPORTED THAT THEIR AED'S ASI IS FLASHING RED, AND REPORTING A SERVICE CODE. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23487799 ↗MalfunctionNov 5, 2025Failure to Power Up; Failure to Power Up
A CUSTOMER REPORTED THAT SEVERAL AEDS AT THEIR FACILITY WERE FOUND TO BE NON-FUNCTIONAL. THE CUSTOMER INDICATED THEY WERE NOT AWARE OF THE MAINTENANCE HISTORY OF THE AFFECTED UNITS. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23481040 ↗MalfunctionNov 5, 2025Failure to Power Up; Failure to Power Up
A CUSTOMER REPORTED THAT SEVERAL AEDS AT THEIR FACILITY WERE FOUND TO BE NON-FUNCTIONAL. THE CUSTOMER INDICATED THEY WERE NOT AWARE OF THE MAINTENANCE HISTORY OF THE AFFECTED UNITS. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23480965 ↗MalfunctionNov 5, 2025Failure to Power Up; Failure to Power Up
A CUSTOMER REPORTED THAT SEVERAL AEDS AT THEIR FACILITY WERE FOUND TO BE NON-FUNCTIONAL. THE CUSTOMER INDICATED THEY WERE NOT AWARE OF THE MAINTENANCE HISTORY OF THE AFFECTED UNITS. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23480964 ↗MalfunctionNov 5, 2025Failure to Power Up; Failure to Power Up
A CUSTOMER REPORTED THAT SEVERAL AEDS AT THEIR FACILITY WERE FOUND TO BE NON-FUNCTIONAL. THE CUSTOMER INDICATED THEY WERE NOT AWARE OF THE MAINTENANCE HISTORY OF THE AFFECTED UNITS. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23480960 ↗MalfunctionOct 24, 2025Premature Discharge of Battery; Premature Discharge of Battery
A CUSTOMER REPORTED THAT THEIR AED'S ASI IS FLASHING RED, AND REPORTING A SERVICE CODE. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23381038 ↗MalfunctionOct 24, 2025Premature Discharge of Battery; Premature Discharge of Battery
A CUSTOMER REPORTED THAT THEIR AED'S ASI IS FLASHING RED, AND REPORTING A SERVICE CODE. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23381035 ↗MalfunctionOct 19, 2025Failure to Power Up; Failure to Power Up
A CUSTOMER REPORTED THAT THEIR AED WILL NOT POWER ON BUT POWERED ON WITH A SPARE BATTERY PACK AND REPORTED A SERVICE CODE. THEY REPORTED THAT THIS DID NOT OCCUR DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23333697 ↗
Other Automated External Defibrillators (Non-Wearable) devices
- NA 861290Philips Medical Systems Hsg · Automated External Defibrillators (Non-Wearable)12 deaths5,167 reports
- NA 861288Philips Medical Systems Hsg · Automated External Defibrillators (Non-Wearable)21 deaths5,015 reports
- NA 861289Philips Medical Systems Hsg · Automated External Defibrillators (Non-Wearable)7 deaths3,385 reports
- R SERIES 30001005201310012Zoll Medical Corporation · Automated external defibrillators (non-wearable)10 deaths1,720 reports
- PHILIPS HeartStart FRxPhilips Electronics North America Corporation · Automated external defibrillators (non-wearable)26 deaths1,586 reports
- LIFEPAK CR2 99512Physio-Control, Inc. · Automated external defibrillators (non-wearable)8 deaths1,502 reports
- Lifeline Configuration DDU-100ADefibtech, L.L.C. · Automated External Defibrillators (Non-Wearable)1 death1,285 reports
- PHILIPS HeartStart FR3Philips Electronics North America Corporation · Automated External Defibrillators (Non-Wearable)10 deaths1,188 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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