VISERA ELITE II VIDEO SYSTEM CENTERRecalls & reported problems across all models
Olympus Medical Systems Corp. · 3 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1,153
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls
- 0
We found 3 models of VISERA ELITE II VIDEO SYSTEM CENTER by Olympus Medical Systems Corp. in the FDA's device registry (GUDID). Together they are named in 1,153 adverse event reports in the FDA's MAUDE database, received between Dec 30, 2020 and Sep 29, 2026 — classified as 3 injuries, 1,150 malfunctions.
The most frequently reported specific device problem is “No Display/Image” (331 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported VISERA ELITE II VIDEO SYSTEM CENTER problems
Device problems
- No Display/Image331
- Communication or Transmission Problem302
- Output Problem116
- Display or Visual Feedback Problem56
- Electrical /Electronic Property Problem47
- Poor Quality Image47
- Erratic or Intermittent Display45
- Failure to Power Up39
Patient problems
- No Clinical Signs, Symptoms or Conditions1,145
- Electric Shock3
- No Consequences Or Impact To Patient3
- No Patient Involvement3
- Insufficient Information1
VISERA ELITE II VIDEO SYSTEM CENTER models
3 models, most reported first. Each model has its own page with its reports, recalls and device details.
- VISERA ELITE II VIDEO SYSTEM CENTER OLYMPUS OTV-S200Confocal Optical Imaging870 reports
- VISERA ELITE II VIDEO SYSTEM CENTER OLYMPUS OTV-S300Endoscopic Video Imaging System/Component, Gastroenterology-Urology158 reports
- VISERA ELITE II VIDEO SYSTEM CENTER OLYMPUS OTV-S200Endoscopic Video Imaging System/Component, Gastroenterology-Urology125 reports
Recent VISERA ELITE II VIDEO SYSTEM CENTER adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026No Display/Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50934172 ↗MalfunctionSep 23, 2026No Display/Image; Failure to Power Up; Optical Problem
The customer reported that the power did not turn on while preparing for use during inspection for use involving an Olympus Video System Center. During the initial evaluation of the returned device, it was observed that the visual field was too dark or too bright and that the video signal output was abnormal. No patient involvement was reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50870325 ↗MalfunctionSep 23, 2026Naturally Worn; Data Problem
The customer reported the video system center had stopped working in the middle of an unspecified procedure. The procedure was completed using a back-up device. No patient harm was reported. During the initial evaluation of the returned device, the reported event was confirmed and related to the internal buffer being full. Also, a worn-out light guide slider switch was found to have caused an intermittent high intensity mode.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50863173 ↗MalfunctionSep 18, 2026No Display/Image; Communication or Transmission Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50831149 ↗MalfunctionSep 18, 2026Communication or Transmission Problem
The customer reported an error message that stated to clean the electrical panels during an unspecified procedure involving an Olympus Video System Center. There was no patient injury reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50817923 ↗MalfunctionSep 18, 2026Communication or Transmission Problem
The customer reported error code E226 during an unspecified procedure with the Olympus Video System Center. No patient injuries occurred.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50817554 ↗MalfunctionSep 17, 2026Communication or Transmission Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50809911 ↗MalfunctionSep 16, 2026Display or Visual Feedback Problem
The customer reported that the light was dim despite being adjusted to the maximum level in both auto and manual modes on an Olympus Video System Center. There was no patient injury reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50790502 ↗MalfunctionSep 15, 2026Erratic or Intermittent Display
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50780766 ↗MalfunctionSep 15, 2026Communication or Transmission Problem
The customer reported an error code E333 during Diagnostic Laryngoscopy completed with the same device involving an Olympus video system center. There was no patient injury reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50773860 ↗MalfunctionSep 11, 2026No Device Output
The customer reported that the device was not functioning during maintenance involving an Olympus Video System Center. There was no patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50738537 ↗MalfunctionSep 11, 2026Unexpected Mode Switch
The customer reported it intermittently entering standby mode including inadvertent button activation during ureteroscopy involving an Olympus video system center. There were no reports of patient harm.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50731930 ↗MalfunctionSep 11, 2026Poor Quality Image
It was reported that the video system center had red lines running through the image. The issue was found during an unspecified diagnostic procedure that was completed using a fiberscope with light source. There were no reports of patient harm.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50726547 ↗MalfunctionSep 10, 2026Communication or Transmission Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50715354 ↗MalfunctionSep 10, 2026Electrical /Electronic Property Problem
The customer reported Inadvertent button activation and Intermittent standby activation during a ureteroscopy procedure involving an Olympus videoprocessor. There was no patient injury reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50713517 ↗
Other Olympus Medical Systems Corp. products
- EVIS EXERA lll COLONOVIDEOSCOPE16 models · 15,013 reports · 7 recalls
- EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE7 models · 13,448 reports · 7 recalls
- EVIS EXERA II ULTRASOUND GASTROVIDEOSCOPE9 models · 8,317 reports · 2 recalls
- EVIS EXERA III BRONCHOVIDEOSCOPE11 models · 6,060 reports · 16 recalls
- EVIS EXERA III XENON LIGHT SOURCE2 models · 6,694 reports
- EVIS EXERA III COLONOVIDEOSCOPE6 models · 6,117 reports · 5 recalls
- EVIS EXERA III DUODENOVIDEOSCOPE OLYMPUS TJF-Q190V2 models · 5,281 reports · 4 recalls
- HD CAMERA HEAD2 models · 5,217 reports
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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