Olympus A20718ARecalls & reported problems
OLYMPUS Winter & Ibe GmbH · Grasping forceps, optical, for 12° and 30° telescope · Class 2
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 04042761029889), received between Nov 2, 2018 and Mar 6, 2026 — classified as 1 injury, 5 malfunctions.
The most frequently reported specific device problem is “Break” (4 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.
Reports received per month
Most reported problems
Device problems
- Break4
- Difficult to Open or Close2
Patient problems
- No Clinical Signs, Symptoms or Conditions5
- Injury1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 6, 2026Break
IT WAS OBSERVED THAT DURING THE DEVICE EVALUATION, THE GRASPING FORCEPS HAD A BROKEN ALBARRAN WIRE. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24539557 ↗MalfunctionFeb 17, 2026Difficult to Open or Close
IT WAS REPORTED THAT THE GRASPING FORCEPS GRABBER DOES NOT CLOSE. THE ISSUE WAS FOUND DURING INSPECTION FOR USE. THERE WERE NO REPORTS OF PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24363141 ↗MalfunctionMar 28, 2025Break; Break
IT WAS REPORTED THE GRASPING FORCEPS WERE BROKEN AND DO NOT RETRACT OR GRASP. THERE WERE NO REPORTS OF PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21721137 ↗MalfunctionFeb 14, 2024Break; Break
IT WAS REPORTED THAT THE GRASPING FORCEPS, OPTICAL, FOR 12° AND 30° TELESCOPE WAS BROKEN. THE ISSUE OCCURRED DURING REPROCESSING FOR AN UNSPECIFIED DIAGNOSTIC PROCEDURE. THERE WERE NO REPORTS OF PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18701966 ↗MalfunctionAug 11, 2022Break; Break
CUSTOMER REPORTED THAT HIS INSTRUMENT BROKE. ACCORDING TO THE REPORT, THE DEVICE BROKE DURING AN UNSPECIFIED PROCEDURE. ACCORDING TO THE REPORTER, THE DOCTOR WAS ABLE TO RETRIEVE ALL THE SHARDS (BROKEN PIECES) AND THERE WAS NO HARM. THERE WAS NO PATIENT HARM, NO USER INJURY REPORTED DUE TO THE EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15211257 ↗InjuryNov 2, 2018Difficult to Open or Close; Difficult to Open or Close
OLYMPUS WAS INFORMED THAT DURING AN UNSPECIFIED PROCEDURE, THE FORCEPS BECAME LOCKED IN THE OPEN POSITION AND DAMAGED THE PATIENT¿S URETHRA. IT IS UNKNOWN IF THE INTENDED PROCEDURE WAS COMPLETED OR IF THE PATIENT WAS TREATED.
Patient problems: Injury
MAUDE report 8034930 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.