Lifeline Pro Configuration DDU-E2400Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10815098020277), received between Jun 7, 2024 and Oct 17, 2025 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Premature Discharge of Battery” (2 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, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 17, 2025Failure to Power Up; Failure 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. THEY REPORTED THIS DID NOT OCCUR DURING PATIENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23328649 ↗
• MalfunctionSep 10, 2025Premature Discharge of Battery; Premature Discharge of Battery

  AN INTERNATIONAL DISTRIBUTOR REPORTED THAT THEIR CUSTOMER'S AED'S BATTERY PACK WAS DEPLETED; HOWEVER, WHEN TESTED WITH A SPARE BATTERY PACK, IT DID POWER ON. THEY REPORTED THIS DID NOT OCCUR DURING PATIENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23018302 ↗
• MalfunctionAug 4, 2025Premature Discharge of Battery; Premature Discharge of Battery

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

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22700180 ↗
• MalfunctionJul 30, 2025Failure to Deliver Shock/Stimulation; Failure to Deliver Shock/Stimulation

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

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22667333 ↗
• MalfunctionJun 7, 2024Battery Problem; Battery Problem

  THE DISTRIBUTOR REPORTED THAT THEIR CUSTOMER REPORTED THAT THEIR AED WOULD NOT TURN ON. THE AED WAS SENT TO THE DISTRIBUTOR, WHO ATTEMPTED TO TURN ON THE DEVICE, BUT THE BATTERY PACK WAS DEPLETED AND THE AED WOULD NOT POWER ON. THE REPORTED EVENT DID NOT OCCUR DURING PATIENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19488739 ↗