VIDEO ADAPTER OLYMPUS A10-T2Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 04953170023422), received between Mar 6, 2024 and Jan 21, 2026 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).

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.

Most reported problems

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionJan 21, 2026Gas/Air Leak

  IT WAS REPORTED THAT THE VIDEO ADAPTER EXHIBITED HAD WATER INVASION. THE EVENT OCCURRED DURING REPROCESSING. THERE WERE NO REPORTS OF PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24133557 ↗
• MalfunctionOct 15, 2024Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS OBSERVED THAT DURING THE DEVICE EVALUATION, THE SUBJECT DEVICE SHOWED WATER INGRESS IN THE MAIN UNIT. THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20450579 ↗
• MalfunctionJun 24, 2024Poor Quality Image; Poor Quality Image

  IT WAS REPORTED THAT THE SUBJECT DEVICE HAD POOR FOCUS AND IMAGE WAS OUT OF FOCUS. THE ISSUE WAS IDENTIFIED DURING PRE-USE INSPECTION. THE INTENDED PROCEDURE WAS COMPLETED. THERE WERE NO REPORTS OF PATIENT HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19601161 ↗
• MalfunctionJun 13, 2024Leak/Splash; Detachment of Device or Device Component; Leak/Splash; Detachment of Device or Device Component

  IT WAS OBSERVED THAT DURING THE DEVICE EVALUATION, THE LENS OF THE MAIN UNIT OF SUBJECT DEVICE WAS FLOODED AND A FRONT COVER SCREW WAS MISSING. THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19531838 ↗
• MalfunctionMar 6, 2024Display or Visual Feedback Problem; Display or Visual Feedback Problem

  THIS REPORT IS BEING SUPPLEMENTED BASED ON ADDITIONAL INFORMATION PROVIDED BY THE COMPLETED INVESTIGATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18847137 ↗