Lifeline View Configuration DDU-E2300Recalls & reported problems
Defibtech, L.L.C. · Class 3
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
Quick summary
This Defibtech Lifeline View defibrillator is an automated external defibrillator used in cardiac arrest. Its 221 reports mostly describe batteries running down early or the unit failing to power on, and some describe service codes or failed shocks. Reports fell sharply in the last 12 months, with 22 compared with 105 in the year before. There is 1 open recall, which began in March 2025 over missing Italian-language labeling for Switzerland.
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
- 221
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 221 adverse event reports that list this exact device (DI 10815098020239), received between Jul 12, 2019 and Jan 23, 2026 — classified as 221 malfunctions.
The most frequently reported specific device problem is “Premature Discharge of Battery” (95 reports).
1 FDA recall record name this device's identifier, 1 still open.
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
Recalls naming this device
- Mar 18, 2025Open, Classified
It was noticed there was no Italian translation included for the AED. Article 16 of the Swiss Medical Devices Ordinance (MedDO) states that product information (labelling and instructions for use) should be provided in all three official languages of Switzerland (German, French, and Italian).
Z-1692-2025 · Root cause: Process control · FDA record ↗
Most reported problems
Device problems
- Premature Discharge of Battery95
- Failure to Power Up94
- Battery Problem19
- Failure to Deliver Shock/Stimulation5
- Electrical /Electronic Property Problem2
- Failure to Sense2
- No Audible Prompt/Feedback2
- No Display/Image2
Patient problems
- No Clinical Signs, Symptoms or Conditions218
- Death1
- Insufficient Information1
- Unspecified Heart Problem1
Recent adverse event reports
The 25 most recent of 221 reports, in the reporter's own words as published by the FDA.
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 24162074 ↗MalfunctionJan 21, 2026Failure to Power Up
AN INTERNATIONAL DISTRIBUTOR REPORTED THAT THEIR CUSTOMER'S AED WOULD NOT POWER ON; HOWEVER, WHEN TESTED WITH A SPARE BATTERY PACK, IT DID POWER 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 24133071 ↗MalfunctionJan 20, 2026Failure to Power Up
AN INTERNATIONAL DISTRIBUTOR REPORTED THEIR CUSTOMER'S AED WOULD NOT POWER ON. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24127119 ↗MalfunctionJan 6, 2026Premature Discharge of Battery
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 23974022 ↗MalfunctionJan 6, 2026Premature 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 23974019 ↗MalfunctionJan 5, 2026Premature Discharge of Battery
AN INTERNATIONAL DISTRIBUTOR REPORTED THAT THEIR CUSTOMER'S BATTERY PACK WAS DEPLETED. WHEN TESTED WITH A SPARE BATTERY PACK, THE AED POWERED. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23963860 ↗MalfunctionJan 5, 2026Premature Discharge of Battery
AN INTERNATIONAL DISTRIBUTOR REPORTED THAT THEIR CUSTOMER'S BATTERY PACK WAS DEPLETED. WHEN TESTED WITH A SPARE BATTERY PACK, THE 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 23963734 ↗MalfunctionJan 5, 2026Premature Discharge of Battery
AN INTERNATIONAL DISTRIBUTOR REPORTED THEIR CUSTOMER'S BATTERY PACK WAS DEPLETED. WHEN TESTED WITH A SPARE BATTERY PACK, THE AED POWER ON. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23963733 ↗MalfunctionDec 21, 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 23860398 ↗MalfunctionDec 18, 2025Premature Discharge of Battery; Premature Discharge of Battery
AN INTERNATIONAL DISTRIBUTOR REPORTED THEIR CUSTOMER'S AED BATTERY WAS DEPLETED. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23839864 ↗MalfunctionDec 18, 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 23839860 ↗MalfunctionDec 17, 2025Failure to Power Up; Failure to Power Up
A CUSTOMER REPORTED THAT THEIR AED'S SCREEN 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 23832234 ↗MalfunctionDec 5, 2025Premature Discharge of Battery; Premature 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 23735191 ↗MalfunctionDec 2, 2025Failure to Power Up; Failure to Power Up
AN INTERNATIONAL DISTRIBUTOR REPORTED THEIR CUSTOMER'S AED BATTERY WAS DEPLETED. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23697716 ↗MalfunctionDec 1, 2025Failure to Power Up; Failure to Power Up
AN INTERNATIONAL DISTRIBUTOR REPORTED THAT THEIR CUSTOMER'S AED WOULD NOT POWER ON; HOWEVER, WHEN TESTED WITH A SPARE BATTERY PACK, IT DID POWER 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 23682736 ↗MalfunctionDec 1, 2025Premature Discharge of Battery; Premature Discharge of Battery
AN INTERNATIONAL DISTRIBUTOR REPORTED THEIR CUSTOMER'S 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 23682646 ↗MalfunctionNov 21, 2025Failure to Power Up; Failure to Power Up
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 23622173 ↗MalfunctionNov 21, 2025Premature Discharge of Battery; Premature Discharge of Battery
A CUSTOMER REPORTED THEIR AED IS FLASHING RED AND PROMPTING A "REPLACE BATTERY PACK NOW" WARNING. THEY REPORTED THIS DID NOT OCCUR DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23622170 ↗MalfunctionNov 18, 2025Premature Discharge of Battery; Premature Discharge of Battery
AN INTERNATIONAL DISTRIBUTOR REPORTED THAT THEIR CUSTOMER'S AED'S BATTERY WAS DEPLETED; HOWEVER, WHEN TESTED WITH A SPARE BATTERY PACK, IT DID POWER ON. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23584929 ↗MalfunctionNov 18, 2025Premature Discharge of Battery; Premature Discharge of Battery
AN INTERNATIONAL DISTRIBUTOR REPORTED THAT THEIR CUSTOMER'S AED'S ASI IS FLASHING RED, AND REPORTING A SERVICE CODE. THEY ALSO REPORTED THE AED'S SCREEN IS BLANK. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23584906 ↗MalfunctionNov 7, 2025Premature Discharge of Battery; Premature Discharge of Battery
A CUSTOMER REPORTED THAT THEIR AED'S ASI IS 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 23497652 ↗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 23487787 ↗MalfunctionOct 30, 2025Premature Discharge of Battery; Premature Discharge of Battery
AN INTERNATIONAL DISTRIBUTOR REPORTED THAT THEIR CUSTOMER'S AED WOULD NOT POWER ON; HOWEVER, WHEN TESTED WITH A SPARE BATTERY PACK, IT DID POWER 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 23429793 ↗MalfunctionOct 27, 2025Failure to Power Up; Failure to Power Up
AN INTERNATIONAL DISTRIBUTOR REPORTED THEIR CUSTOMER'S AED BATTERY WAS DEPLETED AND THE AED WOULD NOT POWER ON. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23393097 ↗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 23381043 ↗
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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.