Lifeline View 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 Lifeline View DDU-E2300 defibrillator from Defibtech is a portable device used to shock the heart during sudden cardiac arrest. The 75 reports mostly describe the battery draining on its own, or the unit failing to power up or show a display; reports rose from 1 in the prior 12 months to 74 in the last 12 months. There are no deaths and 1 injury. One open recall, from March 2025, concerns missing Italian text on the labeling and instructions for use.
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
- 80
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 80 adverse event reports that list this exact device (DI 00815098020232), received between Mar 26, 2025 and Sep 30, 2026 — classified as 1 injury, 79 malfunctions.
The most frequently reported specific device problem is “Premature Discharge of Battery” (51 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 Battery51
- Failure to Power Up20
- Battery Problem3
- Device Sensing Problem3
- No Audible Prompt/Feedback2
- No Display/Image1
Patient problems
- No Clinical Signs, Symptoms or Conditions79
- Insufficient Information1
Recent adverse event reports
The 25 most recent of 80 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Premature Discharge of Battery
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50953770 ↗MalfunctionSep 26, 2026Premature Discharge of Battery
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50908147 ↗MalfunctionSep 26, 2026Failure to Power Up
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50908143 ↗MalfunctionSep 26, 2026Failure to Power Up
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50906478 ↗MalfunctionSep 23, 2026Failure to Power Up
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50873417 ↗MalfunctionSep 22, 2026Failure to Power Up
An international distributor reported that their customer's AED battery was depleted. When tested with a spare battery pack, the AED powered on. The customer did not report this occurring during patient use.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50853442 ↗MalfunctionSep 22, 2026Premature 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 50853441 ↗MalfunctionSep 1, 2026Failure to Power Up
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50545160 ↗MalfunctionSep 1, 2026Failure to Power Up
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50545157 ↗MalfunctionSep 1, 2026Failure to Power Up
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50545153 ↗MalfunctionAug 31, 2026Premature Discharge of Battery
An international distributor reported that their customer's AED screen is blank. The customer did not report this occurring during patient use.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50524487 ↗MalfunctionAug 24, 2026No Audible Prompt/Feedback
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50419052 ↗MalfunctionAug 24, 2026Premature Discharge of Battery
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50419051 ↗MalfunctionAug 12, 2026Premature Discharge of Battery
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50223295 ↗InjuryAug 10, 2026Premature Discharge of Battery
An international distributor reported 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 50195596 ↗MalfunctionAug 6, 2026Premature Discharge of Battery
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50160571 ↗MalfunctionAug 5, 2026Premature Discharge of Battery
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50147539 ↗MalfunctionAug 5, 2026Device Sensing Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50147527 ↗MalfunctionAug 5, 2026Device Sensing Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50147523 ↗MalfunctionAug 5, 2026Premature Discharge of Battery
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50143776 ↗MalfunctionAug 3, 2026Failure to Power Up
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50122806 ↗MalfunctionJul 28, 2026
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50057441 ↗MalfunctionJul 22, 2026Device Sensing Problem
Patient problems: Insufficient Information
MAUDE report 25906964 ↗MalfunctionJul 21, 2026Premature Discharge of Battery
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25899272 ↗MalfunctionJul 21, 2026Premature Discharge of Battery
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25899134 ↗
Other Automated External Defibrillators (Non-Wearable) devices
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- 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.