Lifeline VIEW AUTO Configuration DDU-E2200Recalls & reported problems

Summary

The FDA's MAUDE database contains 11 adverse event reports that list this exact device (DI 10815098020192), received between Jan 18, 2024 and Jan 12, 2026 — classified as 11 malfunctions.

The most frequently reported specific device problem is “Premature Discharge of Battery” (6 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-1694-2025 · 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-1691-2025 · Root cause: Process control · FDA record ↗

Most reported problems

Recent adverse event reports

The 11 most recent of 11 reports, in the reporter's own words as published by the FDA.

• MalfunctionJan 12, 2026Premature Discharge of Battery

  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 24040560 ↗
• MalfunctionDec 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. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23858850 ↗
• MalfunctionDec 12, 2025Premature Discharge of Battery; Premature Discharge of Battery

  AN INTERNATIONAL DISTRIBUTOR REPORTED THAT THEIR CUSTOMER'S 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 23795360 ↗
• MalfunctionNov 21, 2025Power Problem; Power Problem

  AN INTERNATIONAL DISTRIBUTOR REPORTED THAT A CUSTOMER'S AED FAILED TO POWER ON DURING A RESCUE ATTEMPT. ACCORDING TO THE RESCUER, NO RESUSCITATION WAS REQUIRED AT THE TIME OF THE EVENT; HOWEVER, THE EMERGENCY LINE OPERATOR ADVISED THE RESCUER TO POWER ON THE AED AND APPLY THE ELECTRODE PADS TO ASSESS THE PATIENT'S CARDIAC RHYTHM. WHEN ATTEMPTING TO DO SO, THE RESCUER DISCOVERED THAT THE AED WOULD NOT TURN ON. BECAUSE THE DEVICE COULD NOT BE POWERED ON, THE ELECTRODE PADS WERE NOT ATTACHED, AND THE AED WAS NOT USED. EMERGENCY MEDICAL PERSONNEL ARRIVED SHORTLY THEREAFTER AND ASSUMED CARE OF THE PATIENT. NO PATIENT HARM WAS REPORTED. THE AED HAS BEEN REQUESTED FOR RETURN AND EVALUATION.

  Patient problems: Insufficient Information

  MAUDE report 23622152 ↗
• MalfunctionJul 15, 2025Premature Discharge of Battery; Premature Discharge of Battery

  A CUSTOMER REPORTED THEIR AED IS FLASHING RED AND PROMPTING A SERVICE CODE. THEY REPORTED THIS DID NOT OCCUR DURING PATIENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22512405 ↗
• MalfunctionJul 8, 2025Premature Discharge of Battery; Premature Discharge of Battery

  AN INTERNATIONAL DISTRIBUTOR REPORTED A CUSTOMER'S AED IS REPORTING A SERVICE CODE AND THAT THE DISPLAY SCREEN IS BLANK. THEY REPORTED THAT THIS DID NOT OCCUR DURING PATIENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22439524 ↗
• MalfunctionApr 3, 2025Premature Discharge of Battery; Premature Discharge of Battery

  AN INTERNATIONAL DISTRIBUTOR 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. THEY REPORTED THIS DID NOT OCCUR DURING PATIENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21767549 ↗
• MalfunctionOct 25, 2024Defibrillation/Stimulation Problem; Defibrillation/Stimulation Problem

  A CUSTOMER REPORTED THAT THEIR AED SHOCK VALUE IS LOWER THAN 135 JOULES AND FAILED SELF TEST. THEY REPORTED THIS DID NOT OCCUR DURING PATIENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20539280 ↗
• MalfunctionJul 2, 2024Battery Problem; Battery Problem

  AN INTERNATIONAL DISTRIBUTOR REPORTED A SERVICE CODE ON THEIR CUSTOMER'S AED. THEY REPORTED THAT THIS DID NOT OCCUR DURING PATIENT USE. REVIEW OF THE LOG FILES FROM THE AED IDENTIFIED THAT THE SERVICE CODE WOULD NOT CLEAR WITH A MANUAL SELF-TEST AND THUS THE AED WAS REQUESTED TO BE RETURNED SO THAT IT MAY BE EVALUATED AND TESTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19661528 ↗
• MalfunctionMar 15, 2024Failure to Power Up; Failure to Power Up

  A CUSTOMER REPORTED THAT THEIR AED WILL NOT POWER ON BUT POWERED ON WITH A SPARE BATTERY PACK. THEY REPORTED THAT THIS DID NOT OCCUR DURING PATIENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18918729 ↗
• MalfunctionJan 18, 2024Failure to Power Up; Failure to Power Up

  A DISTRIBUTOR REPORTED THEIR CUSTOMER'S AED WOULD NOT POWER ON. THEY REPORTED THAT THIS DID NOT OCCUR DURING PATIENT USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18540018 ↗

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-1693-2025 · Mar 18, 2025 · Open, Classified
  Automated External Defibrillators, Model DDU-2450. Item number: DCF-E2460DE (German language)
• 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-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-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
• 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-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