Olympus A20714ARecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 04042761020022), received between Apr 28, 2025 and Dec 15, 2025 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Break” (2 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 15, 2025Break; Break

  IT WAS REPORTED THAT THE TIP OF THE SHEATH WAS BROKEN. NO HARM REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23803085 ↗
• MalfunctionAug 22, 2025Mechanical Problem; Mechanical Problem

  NO ADDITIONAL INFORMATION RECEIVED FROM THE CUSTOMER

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22873232 ↗
• MalfunctionJul 10, 2025Break; Break

  IT WAS REPORTED THAT THE SUBJECT DEVICE HAD A DETACHED OR BROKEN LINKAGE ON THE FORCEPS (UNABLE TO CLOSE OR OPEN FORCEPS). THE ISSUE OCCURRED DURING A UNKNOWN PROCEDURE. THERE WERE NO REPORTS OF PATIENT HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22469739 ↗
• MalfunctionApr 28, 2025Mechanical Jam; Mechanical Jam

  IT WAS REPORTED THAT THE GRASPING FORCEPS, SECOND WORKING ELEMENT WAS STUCK OPEN WOULD NOT CLOSE. THE ISSUE OCCURRED AT REPROCESSING. THERE WERE NO REPORTS OF PATIENT HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21918772 ↗