Lifeline ViewRecalls & reported problems across all models
Defibtech, L.L.C. · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one Lifeline View model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 119
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls
- 1
We found 2 models of Lifeline View by Defibtech, L.L.C. in the FDA's device registry (GUDID). Together they are named in 119 adverse event reports in the FDA's MAUDE database, received between Mar 26, 2025 and Sep 30, 2026 — classified as 1 injury, 118 malfunctions.
The most frequently reported specific device problem is “Premature Discharge of Battery” (62 reports).
1 FDA recall record name at least one of these models by its device 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Lifeline View recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- 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 · Recall details · FDA record ↗
Most reported Lifeline View problems
Device problems
- Premature Discharge of Battery62
- Failure to Power Up39
- Battery Problem6
- Device Sensing Problem4
- No Audible Prompt/Feedback3
- Failure to Deliver Shock/Stimulation1
- Inappropriate/Inadequate Shock/Stimulation1
- Material Deformation1
Patient problems
- No Clinical Signs, Symptoms or Conditions118
- Insufficient Information1
Lifeline View models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Lifeline View DDU-E2300Automated External Defibrillators (Non-Wearable)1 recall80 reports
- Lifeline View DDU-A2300Automated External Defibrillators (Non-Wearable)39 reports
Recent Lifeline View adverse event reports
The 15 most recent reports across all models, 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 30, 2026Battery Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50953766 ↗MalfunctionSep 29, 2026Premature Discharge of Battery
A customer reported that their AED's 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 50935598 ↗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 50873422 ↗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 14, 2026Failure 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 50755240 ↗MalfunctionSep 2, 2026Failure to Power Up
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50568788 ↗MalfunctionSep 2, 2026Premature Discharge of Battery
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50568786 ↗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 ↗
Other Defibtech, L.L.C. products
- Lifeline Configuration2 models · 1,754 reports · 1 recall
- Lifeline2 models · 817 reports · 2 recalls
- Lifeline Auto Configuration2 models · 430 reports
- Lifeline View Configuration2 models · 335 reports · 1 recall
- Lifeline Auto2 models · 218 reports
- Defibtech ACC Configuration2 models · 80 reports
- Lifeline ECG Configuration2 models · 9 reports · 1 recall
- Lifeline ECG2 models · 4 reports · 1 recall
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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