Lifeline View 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
1 open recall names at least one Lifeline View Configuration model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 335
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 2 models of Lifeline View Configuration by Defibtech, L.L.C. in the FDA's device registry (GUDID). Together they are named in 335 adverse event reports in the FDA's MAUDE database, received between Jun 20, 2019 and Jan 23, 2026 — classified as 335 malfunctions.
The most frequently reported specific device problem is “Premature Discharge of Battery” (144 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 Configuration 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 Configuration problems
Device problems
- Premature Discharge of Battery144
- Failure to Power Up131
- Battery Problem28
- Failure to Deliver Shock/Stimulation13
- Failure to Sense4
- No Audible Prompt/Feedback4
- Display or Visual Feedback Problem3
- No Display/Image3
Patient problems
- No Clinical Signs, Symptoms or Conditions327
- Unspecified Heart Problem4
- Insufficient Information2
- Death1
- No Known Impact Or Consequence To Patient1
Lifeline View Configuration models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Lifeline View Configuration DDU-E2300Automated External Defibrillators (Non-Wearable)1 recall221 reports
- Lifeline View Configuration DDU-A2300Automated External Defibrillators (Non-Wearable)114 reports
Recent Lifeline View Configuration adverse event reports
The 15 most recent reports across all models, 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 23, 2026No Audible Prompt/Feedback
A CUSTOMER REPORTED THEIR AED WILL NOT SPEAK. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24162035 ↗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 24159834 ↗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 12, 2026Premature Discharge of Battery
A CUSTOMER REPORTED A SERVICE CODE. ASI IS FLASHING RED. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24040770 ↗MalfunctionJan 12, 2026Premature Discharge of Battery
A CUSTOMER REPORTED A SERVICE CODE. ASI IS FLASHING RED. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24040749 ↗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 ↗MalfunctionJan 5, 2026No Audible Prompt/Feedback
A CUSTOMER REPORTED THEIR AED WILL NOT SPEAK. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23963730 ↗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 ↗
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 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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