Lifeline Auto ConfigurationRecalls & 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
- Adverse event reports
- 430
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 0
We found 2 models of Lifeline Auto Configuration by Defibtech, L.L.C. in the FDA's device registry (GUDID). Together they are named in 430 adverse event reports in the FDA's MAUDE database, received between Sep 22, 2020 and Aug 10, 2026 — classified as 430 malfunctions.
The most frequently reported specific device problem is “Failure to Power Up” (197 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 Configuration problems
Device problems
- Failure to Power Up197
- Premature Discharge of Battery132
- Battery Problem39
- Failure to Deliver Shock/Stimulation33
- No Audible Prompt/Feedback15
- Inappropriate/Inadequate Shock/Stimulation5
- Failure to Sense4
- Mechanical Problem4
Patient problems
- No Clinical Signs, Symptoms or Conditions422
- Insufficient Information4
- Death2
- Atrial Fibrillation1
- Cancer1
- Cardiac Arrest1
- Unspecified Heart Problem1
Lifeline Auto Configuration models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Lifeline Auto Configuration DDU-120AAutomated External Defibrillators (Non-Wearable)250 reports
- Lifeline Auto Configuration DDU-120EAutomated External Defibrillators (Non-Wearable)180 reports
Recent Lifeline Auto Configuration adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionAug 10, 2026Battery Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50192577 ↗MalfunctionAug 10, 2026Battery Problem
The customer reported the AED did not power on when deployed for a rescue attempt. The reported event occurred during patient use. The customer stated that they rarely need to use AEDs, so it wasn't being maintained at all. This patient had terminal cancer and when their AED did not power on EMS tried to use their AED (not Defibtech) and he did not have a shockable rhythm and no shock was advised nor delivered. The patient was pronounced dead at the hospital. Although the patient was not resuscitated in this case, the patient's death is not attributed to this device problem.
Patient problems: Cancer; Unspecified Heart Problem
MAUDE report 50192576 ↗MalfunctionJan 23, 2026Premature Discharge of Battery
A CUSTOMER REPORTED THAT THEIR AED'S BATTERY WAS DEPLETED. WHEN TESTED WITH A SPARE BATTERY PACK, IT 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 24164957 ↗MalfunctionJan 23, 2026Failure to Power Up
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 24164912 ↗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 24159832 ↗MalfunctionJan 23, 2026Premature Discharge of Battery
A CUSTOMER REPORTED THAT THEIR 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 24159813 ↗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 24159812 ↗MalfunctionJan 22, 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 24152385 ↗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 24133068 ↗MalfunctionJan 20, 2026Failure to Power Up
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 24127113 ↗MalfunctionJan 15, 2026Failure to Power Up
A CUSTOMER REPORTED THAT THEIR 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 24085111 ↗MalfunctionJan 13, 2026Failure to Power Up
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 24055225 ↗MalfunctionJan 13, 2026Battery Problem
AN INTERNATIONAL DISTRIBUTOR REPORTED A CUSTOMER'S BATTERY PACK WILL NOT STAY LATCHED IN THEIR AED. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24052889 ↗MalfunctionJan 13, 2026Premature Discharge of Battery
AN INTERNATIONAL DISTRIBUTOR REPORTED THEIR CUSTOMER'S AED 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 24052864 ↗MalfunctionJan 6, 2026Premature 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 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 23979778 ↗
Other Defibtech, L.L.C. products
- Lifeline Configuration2 models · 1,754 reports · 1 recall
- Lifeline2 models · 817 reports · 2 recalls
- Lifeline View Configuration2 models · 335 reports · 1 recall
- Lifeline Auto2 models · 218 reports
- 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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