Lifeline ECG ConfigurationRecalls & reported problems across all models

We found 2 models of Lifeline ECG Configuration by Defibtech, L.L.C. in the FDA's device registry (GUDID). Together they are named in 9 adverse event reports in the FDA's MAUDE database, received between Aug 15, 2021 and Oct 15, 2025 — classified as 9 malfunctions.

The most frequently reported specific device problem is “Failure to Power Up” (4 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

Lifeline ECG 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.

1. 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-1693-2025 · Root cause: Process control · Recall details · FDA record ↗

Most reported Lifeline ECG Configuration problems

Lifeline ECG Configuration models

2 models, most reported first. Each model has its own page with its reports, recalls and device details.

• Lifeline ECG Configuration DDU-E2450

  Automated External Defibrillators (Non-Wearable)
  1 recall2 reports
• Lifeline ECG Configuration DDU-A2450

  Automated External Defibrillators (Non-Wearable)
  7 reports

Recent Lifeline ECG Configuration adverse event reports

The 9 most recent reports across all models, in the reporter's own words as published by the FDA.

• MalfunctionOct 15, 2025Failure to Power Up; Failure to Power Up

  A CUSTOMER REPORTED THAT THEIR AED'S ASI IS FLASHING RED, AND IT WILL NOT POWER ON. THEY REPORTED THAT THIS DID NOT OCCUR DURING PATIENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23301882 ↗
• MalfunctionAug 26, 2025Failure to Power Up; Failure to Power Up

  A CUSTOMER REPORTED THAT THEIR AED'S ASI IS BLANK, AND THE AED WILL NOT POWER ON. THEY REPORTED THAT THIS DID NOT OCCUR DURING PATIENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22901061 ↗
• MalfunctionAug 25, 2025Premature Discharge of Battery; Premature Discharge of Battery

  A CUSTOMER REPORTED THAT THEIR AED'S ASI IS FLASHING RED AND REPORTING A SERVICE CODE. THEY REPORTED THAT THIS DID NOT OCCUR DURING PATIENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22889267 ↗
• MalfunctionAug 25, 2025Premature Discharge of Battery; Premature Discharge of Battery

  A CUSTOMER REPORTED THAT THEIR AED'S ASI IS FLASHING RED, AND REPORTING A SERVICE CODE. THEY REPORTED THAT THIS DID NOT OCCUR DURING PATIENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22889248 ↗
• MalfunctionAug 20, 2025Premature Discharge of Battery; Premature Discharge of Battery

  A CUSTOMER REPORTED THAT THEIR AED'S ASI IS FLASHING RED AND REPORTING A SERVICE CODE. THEY REPORTED THAT THIS DID NOT OCCUR DURING PATIENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22854087 ↗
• MalfunctionJul 22, 2025Failure to Sense; Failure to Sense

  A CUSTOMER REPORTED THEIR PADS ARE NOT RECOGNIZED BY THE AED. THEY REPORTED THIS DID NOT OCCUR DURING PATIENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22564422 ↗
• MalfunctionOct 16, 2024Failure to Power Up; Failure to Power Up

  THE CUSTOMER REPORTED THAT THE AED WILL NOT POWER ON AND IT WOULD NOT POWER ON EVEN WITH THE TEST BATTERY. THEY REPORTED THIS DID NOT OCCUR DURING PATIENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20464907 ↗
• MalfunctionAug 17, 2024Failure to Power Up; Battery Problem; Failure to Power Up; Battery Problem

  THE DISTRIBUTOR REPORTED FOR THEIR CUSTOMER THAT THE AED IS DEPLETING BATTERIES PREMATURELY. THIS IS THE SECOND BATTERY PACK TO BE DEPLETED BEFORE ITS EXPIRATION DATE. THE CUSTOMER DID NOT REPORT THIS EVENT OCCURRED DURING PATIENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19998801 ↗
• MalfunctionAug 15, 2021Display or Visual Feedback Problem; Display or Visual Feedback Problem

  A CUSTOMER REPORTED THAT THEY RECEIVED AN E-MAIL FROM A RESCUER THAT THE DEFIBRILLATOR DID NOT WORK ON A PASSENGER AND THAT THE AED COUNTED DOWN BUT WOULD NOT PROVIDE VITALS. NO ADDITIONAL INFORMATION WAS AVAILABLE.

  Patient problems: Insufficient Information

  MAUDE report 12322348 ↗

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
• Lifeline View2 models · 119 reports · 1 recall
• Defibtech ACC Configuration2 models · 80 reports
• Lifeline ECG2 models · 4 reports · 1 recall