ReviveR View Configuration DDU-C2300Recalls & reported problems
Defibtech, L.L.C. · Class 3
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Quick summary
This Defibtech ReviveR defibrillator appears in 92 adverse event reports, with no deaths and no injuries. Reports mostly describe the unit failing to power on and batteries draining early, with service codes showing up. Some reports note the problem did not occur during patient use. There were 17 reports in the past 12 months, down from 52 in the year before. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 92
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 92 adverse event reports that list this exact device (DI 10815098020222), received between Nov 19, 2019 and Jan 23, 2026 — classified as 92 malfunctions.
The most frequently reported specific device problem is “Failure to Power Up” (37 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Failure to Power Up37
- Premature Discharge of Battery33
- Battery Problem7
- Failure to Sense4
- Failure to Deliver Shock/Stimulation3
- No Audible Prompt/Feedback2
- Complete Loss of Power1
- Connection Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions89
- Insufficient Information2
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 25 most recent of 92 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 23, 2026Premature Discharge of Battery
A CUSTOMER 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. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24164924 ↗MalfunctionJan 21, 2026Failure to Power Up
A CUSTOMER 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. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24136460 ↗MalfunctionJan 15, 2026Failure to Power Up
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 24085086 ↗MalfunctionDec 18, 2025Failure to Power Up; Failure to Power Up
A CUSTOMER REPORTED THAT THEIR AED'S BATTERY WAS DEPLETED. WHEN TESTED WITH A SPARE BATTERY PACK, IT 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 23843107 ↗MalfunctionDec 18, 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. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23840489 ↗MalfunctionDec 18, 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. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23840488 ↗MalfunctionDec 12, 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 23795445 ↗MalfunctionDec 12, 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 23795444 ↗MalfunctionDec 10, 2025Failure to Power Up; Failure to Power Up
A CUSTOMER REPORTED THAT THEIR AED'S ASI IS FLASHING RED, 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 23773912 ↗MalfunctionDec 9, 2025Premature Discharge of Battery; Premature Discharge of Battery
A CUSTOMER REPORTED THEIR AED IS FLASHING RED AND PROMPTING A "REPLACE BATTERY PACK NOW" WARNING. THEY REPORTED THIS DID NOT OCCUR DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23764540 ↗MalfunctionDec 9, 2025Inaudible or Unclear Audible Prompt/Feedback; Inaudible or Unclear 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 23760496 ↗MalfunctionDec 5, 2025Failure to Sense; Failure to Sense
A CUSTOMER REPORTED THEIR PADS ARE NOT RECOGNIZED BY THE AED. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23735172 ↗MalfunctionNov 21, 2025Failure to Power Up; Failure to Power Up
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 23622191 ↗MalfunctionNov 15, 2025Failure to Sense; Failure to Sense
CUSTOMER REPORTED THE AED DID NOT OPERATE PROPERLY DURING A RESCUE. LIMITED EVENT DETAILS WERE AVAILABLE AT THE TIME OF THE CALL, AND THE AED WAS NOT IN THEIR POSSESSION. CUSTOMER ALSO REPORTED A SERVICE CODE 5251, BUT IT WAS UNCLEAR WHETHER THE SC OCCURRED BEFORE, DURING, OR AFTER THE EVENT. CUSTOMER CONFIRMED NO DEATH ASSOCIATED WITH THE INCIDENT.
Patient problems: Insufficient Information
MAUDE report 23564016 ↗MalfunctionNov 12, 2025Failure 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. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23536833 ↗MalfunctionNov 10, 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. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23515261 ↗MalfunctionNov 7, 2025Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
A CUSTOMER REPORTED THAT THEIR AED'S ASI IS FLASHING RED, AND THE AED 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 23500548 ↗MalfunctionOct 31, 2025Premature Discharge of Battery; Premature 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 23436912 ↗MalfunctionOct 30, 2025Failure to Power Up; Failure to Power Up
A CUSTOMER REPORTED THAT THEIR AED'S ASI IS FLASHING RED, 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 23429782 ↗MalfunctionOct 25, 2025Failure to Power Up; Failure to Power Up
A CUSTOMER REPORTED THAT THEIR AED'S ASI IS FLASHING RED, AND THE AED WILL NOT WORK. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23386936 ↗MalfunctionOct 25, 2025Battery Problem; Battery Problem
A CUSTOMER REPORTED THAT THEIR AED'S BATTERY WAS DEPLETED. WHEN TESTED WITH A SPARE BATTERY PACK, IT 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 23386931 ↗MalfunctionOct 24, 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 23381041 ↗MalfunctionOct 23, 2025Premature Discharge of Battery; Premature 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 23371986 ↗MalfunctionOct 18, 2025Premature Discharge of Battery; Premature Discharge of Battery
A CUSTOMER REPORTED THAT UPON INSERTING A NEW BATTERY PACK, THEIR AED POWERED 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 23332818 ↗MalfunctionOct 18, 2025Premature Discharge of Battery; Premature Discharge of Battery
A CUSTOMER REPORTED THAT UPON INSERTING A NEW BATTERY PACK, THEIR AED POWERED 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 23332816 ↗
Other Automated External Defibrillators (Non-Wearable) devices
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- NA 861289Philips Medical Systems Hsg · Automated External Defibrillators (Non-Wearable)7 deaths3,385 reports
- R SERIES 30001005201310012Zoll Medical Corporation · Automated external defibrillators (non-wearable)10 deaths1,720 reports
- PHILIPS HeartStart FRxPhilips Electronics North America Corporation · Automated external defibrillators (non-wearable)26 deaths1,586 reports
- LIFEPAK CR2 99512Physio-Control, Inc. · Automated external defibrillators (non-wearable)8 deaths1,502 reports
- Lifeline Configuration DDU-100ADefibtech, L.L.C. · Automated External Defibrillators (Non-Wearable)1 death1,285 reports
- PHILIPS HeartStart FR3Philips Electronics North America Corporation · Automated External Defibrillators (Non-Wearable)10 deaths1,188 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- 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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