Olympus A20917ARecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04042761030076), received between Mar 8, 2023 and Feb 20, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Crack” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 20, 2026Loose or Intermittent Connection

  IT WAS OBSERVED THAT DURING THE DEVICE EVALUATION, THE RIGID SCOPE PRESENTED LOOSE OBJECTIVE LENS. THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24405283 ↗
• MalfunctionMar 8, 2023Crack; Crack

  THE CUSTOMER REPORTED TO OLYMPUS, THE CYSTOSCOPE 30 DEGREE HAD A CRACKED LENS. THE ISSUE WAS FOUND DURING REPROCESSING. THERE WERE NO REPORTS OF PATIENT HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16506873 ↗