VIDEO ADAPTER OLYMPUS A10-T1Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04953170023392), received between May 31, 2022 and May 31, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Reprocessing Problem” (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 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 31, 2022Device Reprocessing Problem; Device Reprocessing Problem

  THE CUSTOMER ORIGINALLY RETURNED HER OLYMPUS VIDEO ADAPTER DUE TO A FOCUSING ISSUE. DURING THE DEVICE EVALUATION, IT WAS DISCOVERED THAT THE SUBJECT DEVICE HAD UNDERGONE INSUFFICIENT REPROCESSING AS BIOLOGICAL FOREIGN MATERIAL WAS FOUND IN THE AIR/WATER WAY. THIS REPORT IS BEING SUBMITTED TO CAPTURE THE INSUFFICIENT REPROCESSING FOUND DURING THE DEVICE EVALUATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14550712 ↗