Olympus A2580Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04042761003742), received between Jan 18, 2023 and Jan 18, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionJan 18, 2023Break; Break

  OLYMPUS (OEKG) WAS INFORMED THAT THE CUSTOMER FLEXIBLE GRASPING FORCEPS FOR STONE FRAGMENTS WAS RETURNED TO THE OLYMPUS SERVICE DEPARTMENT FOR A REPORTED ¿BROKEN, FOREIGN MATERIAL¿. THE CUSTOMER REPORTED PROBLEM WAS FOUND AT AN UNSPECIFIED EVENT. THE INITIAL INSPECTION FOUND A PART OF THE WORKING END IS BROKEN, THERE IS NO CONNECTION TO THE JAW AND THE GRASPER IS NON-FUNCTIONAL. NO DEATH OR INJURY AND NO IMPACT TO PATIENT OR OTHER HAS BEEN REPORTED TO OLYMPUS. THE DEVICE WILL BE FORWARDED TO THE REGIONAL REPAIR CENTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16192585 ↗