VISERA S VIDEO SYSTEM CENTER OLYMPUS OTV-S500Recalls & reported problems
Olympus Medical Systems Corp. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 04953170454141), received between Sep 2, 2025 and Aug 27, 2026 — classified as 9 malfunctions.
The most frequently reported specific device problem is “No Display/Image” (5 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/Image5
- Poor Quality Image2
- Display or Visual Feedback Problem1
- No Device Output1
Patient problems
- No Clinical Signs, Symptoms or Conditions9
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 27, 2026No Display/Image
The customer reported no image with a Video system center. The event occurred during inspection for use. There was no patient injury reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50467875 ↗MalfunctionAug 18, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50306806 ↗MalfunctionJul 30, 2026No Device Output
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50083849 ↗MalfunctionJan 9, 2026Poor Quality Image
IT WAS REPORTED THE VIDEO SYSTEM CENTER PRESENTED A PINK IMAGE. THE ISSUE OCURRED DURING INSPECTION FOR USE. THERE WERE NO REPORTS OF PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24026818 ↗MalfunctionJan 2, 2026Display or Visual Feedback Problem
NO ADDITIONAL INFORMATION RECEIVED FROM THE CUSTOMER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23946307 ↗MalfunctionDec 11, 2025No Display/Image; No Display/Image
NO ADDITIONAL INFORMATION RECEIVED FROM THE CUSTOMER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23778986 ↗MalfunctionDec 1, 2025No Display/Image; No Display/Image
IT WAS REPORTED THAT THE VIDEO PROCESSOR HAD A FUZZY ENDOSCOPIC IMAGE DURING INSTALLATION. THERE WERE NO REPORTS OF PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23687629 ↗MalfunctionSep 11, 2025No Display/Image; No Display/Image
NO ADDITIONAL INFORMATION RECEIVED FROM THE CUSTOMER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23027913 ↗MalfunctionSep 2, 2025No Display/Image; No Display/Image
NO ADDITIONAL INFORMATION RECEIVED FROM THE CUSTOMER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22936834 ↗
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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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