Lifeline AutoRecalls & reported problems across all models
Defibtech, L.L.C. · 2 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 218
- Deaths reported
- 1
- Injuries reported
- 4
- Recalls
- 0
We found 2 models of Lifeline Auto by Defibtech, L.L.C. in the FDA's device registry (GUDID). Together they are named in 218 adverse event reports in the FDA's MAUDE database, received between Dec 3, 2019 and Sep 30, 2026 — classified as 1 death, 4 injuries, 213 malfunctions.
The most frequently reported specific device problem is “Failure to Power Up” (110 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. 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
Most reported Lifeline Auto problems
Device problems
- Failure to Power Up110
- Premature Discharge of Battery82
- Battery Problem9
- Failure to Deliver Shock/Stimulation7
- No Audible Prompt/Feedback6
- Device Sensing Problem1
- Inappropriate/Inadequate Shock/Stimulation1
- Loss of or Failure to Bond1
Patient problems
- No Clinical Signs, Symptoms or Conditions215
- Insufficient Information2
- No Known Impact Or Consequence To Patient1
Lifeline Auto models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Lifeline Auto DDU-120EAutomated External Defibrillators (Non-Wearable)111 reports
- Lifeline Auto DDU-120AAutomated External Defibrillators (Non-Wearable)1 death107 reports
Recent Lifeline Auto 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 50953767 ↗MalfunctionSep 30, 2026Failure to Power Up
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50951836 ↗MalfunctionSep 29, 2026Premature Discharge of Battery
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50935603 ↗MalfunctionSep 29, 2026Premature Discharge of Battery
A customer reported their AED's ASI is flashing red and prompting a "replace battery pack now" warning. The customer did not report this occurring during patient use.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50935594 ↗MalfunctionSep 29, 2026Failure to Power Up
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 50927994 ↗MalfunctionSep 29, 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. The customer did not report this occurring during patient use.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50927979 ↗MalfunctionSep 25, 2026Failure to Power Up
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50903602 ↗MalfunctionSep 25, 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 50892890 ↗MalfunctionSep 22, 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 50855972 ↗MalfunctionSep 22, 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 50853437 ↗MalfunctionSep 17, 2026Premature Discharge of Battery
A customer reported that their AED's ASI is flashing red, and the device is reporting a battery low warning. The customer did not report this occurring during patient use.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50805454 ↗MalfunctionSep 17, 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 50805452 ↗MalfunctionSep 16, 2026Premature Discharge of Battery
An international distributor reported their customer's AED ASI is flashing red, and the device is reporting a battery low warning. The customer did not report this occurring during patient use.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50790252 ↗MalfunctionSep 16, 2026Failure 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 50790251 ↗MalfunctionSep 15, 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 50772002 ↗
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 View2 models · 119 reports · 1 recall
- 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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