Lifeline VIEW AUTO DDU-E2200Recalls & reported problems

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00815098020195), received between Jun 2, 2026 and Sep 29, 2026 — classified as 8 malfunctions.

The most frequently reported specific device problem is “Premature Discharge of Battery” (5 reports).

2 FDA recall records name this device's identifier, 2 still open.

7 other recalls cover devices cleared under the same FDA submission (P160032); they may or may not involve this specific model.

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.

Recalls naming this device

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-1691-2025 · Root cause: Process control · FDA record ↗

2. 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-1694-2025 · Root cause: Process control · FDA record ↗

Most reported problems

Recent adverse event reports

The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

• 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 50927991 ↗
• MalfunctionSep 29, 2026Premature Discharge of Battery

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50927986 ↗
• MalfunctionAug 31, 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 50524481 ↗
• MalfunctionAug 5, 2026Premature Discharge of Battery

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50147545 ↗
• MalfunctionJul 21, 2026Premature Discharge of Battery

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25891234 ↗
• MalfunctionJul 2, 2026Connection Problem

  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 25693140 ↗
• MalfunctionJun 3, 2026Premature Discharge of Battery

  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 25376615 ↗
• MalfunctionJun 2, 2026Premature Discharge of Battery; Failure to Power Up

  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 25363519 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under P160032. One submission often covers many models, so check the product and lot details in each record.

• Z-1692-2025 · Mar 18, 2025 · Open, Classified
  Automated External Defibrillators, Model DDU-2300. Item numbers: DCF-E2310D3/1(German/English dual language), DCF-E2310E3/1(German/French dual language), DCF-E2310F3/1 (French/Engl
• Z-1690-2025 · Mar 18, 2025 · Open, Classified
  Semi-Automated External Defibrillators; Models: DDU-100 and DDU-100E. Item numbers: DCF-E110SG-DE/1 (German language), DCF-E110SG-FR/1 (French language), DCF-E110SG-IT/1 (Italian l
• Z-1693-2025 · Mar 18, 2025 · Open, Classified
  Automated External Defibrillators, Model DDU-2450. Item number: DCF-E2460DE (German language)
• Z-0504-2025 · Oct 14, 2024 · Open, Classified
  Defibtech DDP-2001: Adult Defibrillation Pads For use with AED Models: Lifeline View Auto, lifeline Pro, lifeline ECG, lifeline View (DDU-2XXX Series). -Indicated for use on victi
• Z-0502-2025 · Oct 14, 2024 · Open, Classified
  Defibtech DDP-100 Adult Defibrillation Pads For use with AED Models: Lifeline and Lifeline Auto (DDU-1:XX Series)- Indicated for use on victims of sudden cardiac arrest (SCA)
• Z-0503-2025 · Oct 14, 2024 · Open, Classified
  Defibtech DDP-200P: Pediatric Defibrillation Pads 0 For use with AED Models: Lifeline and Lifeline Auto (DDU-l XX Series)-Indicated for use on victims of sudden cardiac arrest (SCA
• Z-0505-2025 · Oct 14, 2024 · Open, Classified
  Defibtech DDP-2002: Pediatric Defibrillation Pads For use with AED Models: Lifeline View Auto, lifeline Pro, Lifeline ECG, Lifeline View (DDU-2XXX Series -Indicated for use on