HIGH DEFINITION LCD MONITOR OEV262HRecalls & reported problems
Olympus Medical Systems Corp. · "OEV-262H HIGH DEFINITION LED L CD MONITO" · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This Olympus high-definition LCD monitor shows images from surgical scopes. Many reports describe no display or image, failure to power up, and flickering or intermittent screens. The records include 1,932 reports, 5 injuries and no deaths, 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
- 1,937
- Deaths reported
- 0
- Injuries reported
- 5
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1,937 adverse event reports that list this exact device (DI 04953170363498), received between Sep 20, 2019 and Sep 28, 2026 — classified as 5 injuries, 1,932 malfunctions.
The most frequently reported specific device problem is “No Display/Image” (1,019 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
- No Display/Image1,019
- Failure to Power Up405
- Power Problem143
- Erratic or Intermittent Display99
- Loss of Power99
- Poor Quality Image45
- Electrical /Electronic Property Problem44
- Intermittent Loss of Power40
Patient problems
- No Clinical Signs, Symptoms or Conditions1,870
- No Consequences Or Impact To Patient42
- No Patient Involvement23
- No Known Impact Or Consequence To Patient3
- No Information2
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Bone Cement Implantation Syndrome1
- Insufficient Information1
Recent adverse event reports
The 25 most recent of 1,937 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 28, 2026No Display/Image
The customer reported no image involving an Olympus monitor. There was no patient injury reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50917693 ↗MalfunctionSep 23, 2026Failure to Power Up
The customer reported the display isn¿t powering during an inspection for use involving an Olympus monitor. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50872922 ↗MalfunctionSep 15, 2026Activation Failure
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50780075 ↗MalfunctionSep 15, 2026No Display/Image
The customer reported the high-definition LCD monitor had no image during Inspection for use. During the initial evaluation of the device it was observed, faulty Printed circuit board. No patient involvement was reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50776288 ↗MalfunctionSep 15, 2026No Display/Image
The customer reported no image during maintenance involving an Olympus high definition LCD monitor. There was no patient involvement reported
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50775403 ↗MalfunctionSep 2, 2026No Display/Image; Failure to Power Up
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50573011 ↗MalfunctionAug 31, 2026No Display/Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50523702 ↗MalfunctionAug 27, 2026Failure to Power Up
The customer returned the high-definition liquid crystal display (LCD) monitor for a separate issue. During the initial evaluation of the returned device, it was found that the faulty output signal power caused the unit to shut down. No patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50484424 ↗MalfunctionAug 14, 2026Display or Visual Feedback Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50257875 ↗MalfunctionAug 10, 2026Failure to Power Up
The customer reported no power during a Inspection for use involving an Olympus high definition lcd monitor. There was no patient injury reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50196602 ↗MalfunctionAug 10, 2026No Display/Image; Poor Quality Image
The customer reported a half-screen pink display with no image displayed involving an Olympus High-Definition (LCD) Monitor. There was no patient injury reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50195665 ↗MalfunctionAug 7, 2026Connection Problem
The customer reported Digital Visual Interface (DVI) 1 port was not working, involving an Olympus High Definition LCD Monitor. There was no patient injury reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50181884 ↗MalfunctionAug 7, 2026No Display/Image; Failure to Power Up
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50175081 ↗MalfunctionAug 6, 2026No Display/Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50160999 ↗MalfunctionAug 4, 2026No Display/Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50132182 ↗MalfunctionJul 30, 2026Failure to Select Signal
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50084175 ↗MalfunctionJul 29, 2026No Display/Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50073213 ↗MalfunctionJul 29, 2026Output Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50070162 ↗MalfunctionJul 28, 2026Failure to Power Up
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50053346 ↗MalfunctionJul 27, 2026No Display/Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50037071 ↗MalfunctionJul 15, 2026No Display/Image
THE CUSTOMER REPORTED NO DISPLAY DURING INSPECTION FOR USE INVOLVING AN OLYMPUS HIGH DEFINITION LIQUID CRYSTAL DISPLAY MONITOR. THERE WAS NO PATIENT INVOLVEMENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25825573 ↗MalfunctionJul 14, 2026Erratic or Intermittent Display
THE CUSTOMER REPORTED INTERMITTENT DISPLAY ERRORS, WITH THE DISPLAY CUTTING OUT DURING INSPECTION FOR USE INVOLVING AN OLYMPUS HIGH DEFINITION LIQUID CRYSTAL DISPLAY MONITOR. THERE WAS NO PATIENT HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25813776 ↗MalfunctionJul 8, 2026No Display/Image
THE CUSTOMER REPORTED MONITOR WAS NOT DISPLAYING ANY IMAGE,BOTH SDI PORTS ARE NOT ACCEPTING SIGNAL DURING INSPECTION FOR USE INVOLVING AN OLYMPUS HIGH DEFINITION LIQUID CRYSTAL DISPLAY MONITOR. THERE WAS NO PATIENT INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25751424 ↗MalfunctionJun 28, 2026Power Problem
THE CUSTOMER RETURNED THE HIGH DEFINITION LIQUID CRYSTAL DISPLAY MONITOR, AN OLYMPUS ASSET, WITH NO REPORTED COMPLAINT. DURING THE EVALUATION OF THE DEVICE, IT WAS OBSERVED THAT THE MONITOR SHUT OFF AFTER MINUTES OF OPERATION. THE ISSUE WAS IDENTIFIED BY THE SERVICE REPAIR TECHNICIAN. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25647321 ↗MalfunctionJun 25, 2026Unexpected Shutdown
IT WAS REPORTED DURING AN UNKNOWN PROCEDURE THAT THE MONITOR KEPT OVERHEATING AND TURNING OFF RESULTING IN A DELAY LESS THAN 30 MINUTES. THERE WERE NO REPORTS OF PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25623489 ↗
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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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