ReviveR View DDU-C2300Recalls & reported problems
Defibtech, L.L.C. · Class 3
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This Defibtech ReviveR View DDU-C2300 is an automated external defibrillator (AED). The 34 reports mostly describe the unit failing to power on or its battery pack running down or expiring, sometimes with a blank or flashing red indicator light; all reports were about equipment rather than a patient, and none occurred during patient use. There are 34 malfunction reports, no deaths and no injuries, and 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
- 36
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 36 adverse event reports that list this exact device (DI 00815098020225), received between Feb 9, 2026 and Sep 23, 2026 — classified as 36 malfunctions.
The most frequently reported specific device problem is “Failure to Power Up” (16 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Failure to Power Up16
- Premature Discharge of Battery14
- No Audible Prompt/Feedback2
- Audible Prompt/Feedback Problem1
- Battery Problem1
- Device Sensing Problem1
- Failure to Deliver Shock/Stimulation1
Patient problems
- No Clinical Signs, Symptoms or Conditions36
Recent adverse event reports
The 25 most recent of 36 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 23, 2026Failure to Power Up
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50873436 ↗MalfunctionSep 22, 2026Failure to Power Up
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50859371 ↗MalfunctionSep 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 50772005 ↗MalfunctionSep 14, 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 50753867 ↗MalfunctionSep 3, 2026Failure 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 50589265 ↗MalfunctionAug 26, 2026Device Sensing Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50463615 ↗MalfunctionAug 25, 2026Premature Discharge of Battery
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50436181 ↗MalfunctionAug 11, 2026Failure to Power Up
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50203275 ↗MalfunctionJul 10, 2026Premature Discharge of Battery
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25783101 ↗MalfunctionJul 1, 2026Failure to Power Up
A CUSTOMER REPORTED THAT THEIR AED'S ASI IS BLANK, AND THE AED WILL NOT POWER ON. THE BATTERY PACK INSTALLED IN THE AED WAS EXPIRED AS OF (B)(6) 2026. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25682096 ↗MalfunctionJun 27, 2026Failure 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 25647125 ↗MalfunctionJun 26, 2026Premature Discharge of Battery
A CUSTOMER REPORTED THAT THEIR AED'S BATTERY WAS DEPLETED. WHEN TESTED WITH A SPARE BATTERY PACK, THE 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 25638852 ↗MalfunctionJun 23, 2026Premature Discharge of Battery
A CUSTOMER REPORTED THAT THEIR AED BATTERY WAS DEPLETED. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25597693 ↗MalfunctionJun 20, 2026Premature Discharge of Battery
A CUSTOMER REPORTED THAT THEIR AED'S BATTERY WAS DEPLETED. WHEN TESTED WITH A SPARE BATTERY PACK, THE 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 25571634 ↗MalfunctionJun 20, 2026Premature Discharge of Battery
A CUSTOMER REPORTED THEIR AED'S ASI IS FLASHING RED AND PROMPTING A "REPLACE BATTERY PACK NOW" WARNING. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25571632 ↗MalfunctionJun 19, 2026Premature Discharge of Battery
A CUSTOMER REPORTED THEIR AED'S ASI IS FLASHING RED AND PROMPTING A "REPLACE BATTERY PACK NOW" WARNING. THE CUSTOMER DID NOT REPORT THIS OCCURRING DURING PATIENT USE. DURING TROUBLESHOOTING OF THE DEVICE WITH CUSTOMER SERVICE IT WAS FOUND THAT THE AED WOULD NOT POWER ON.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25563709 ↗MalfunctionJun 3, 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 25376624 ↗MalfunctionJun 2, 2026Premature Discharge of Battery
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 25363518 ↗MalfunctionMay 28, 2026Failure 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 25319745 ↗MalfunctionMay 21, 2026Battery Problem
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 25246181 ↗MalfunctionMay 21, 2026Premature 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 25243709 ↗MalfunctionMay 21, 2026Premature 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 25243702 ↗MalfunctionMay 19, 2026Audible Prompt/Feedback 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 25222439 ↗MalfunctionMay 18, 2026No 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 25209924 ↗MalfunctionMay 18, 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 25209913 ↗
Other Automated External Defibrillators (Non-Wearable) devices
- NA 861290Philips Medical Systems Hsg · Automated External Defibrillators (Non-Wearable)12 deaths5,167 reports
- NA 861288Philips Medical Systems Hsg · Automated External Defibrillators (Non-Wearable)21 deaths5,015 reports
- 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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