DISPOSABLE GRASPING FORCEPS(PARALLEL BASKET TYPE,3Fr.) FG-55DRecalls & reported problems
Olympus Medical Systems Corp. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04953170078934), received between Aug 17, 2022 and Aug 18, 2022 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Difficult to Open or Close” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Difficult to Open or Close2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 18, 2022Difficult to Open or Close; Difficult to Open or Close
THE CUSTOMER REPORTED THAT, DURING A PROCEDURE, WHEN TRYING TO OPEN THE BASKET OF THE SUBJECT DEVICE, THE HANDLE MOVED BUT THE BASKET DID NOT MOVE AND COULD NOT BE CLOSED. THE PROCEDURE WAS COMPLETED BY COLLECTING THE BASKET AND REPLACING IT WITH ANOTHER PRODUCT. THERE WAS NO EFFECT ON THE PATIENT DUE TO THE EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15250556 ↗MalfunctionAug 17, 2022Difficult to Open or Close; Difficult to Open or Close
THE CUSTOMER REPORTED THAT, DURING A PROCEDURE, WHEN TRYING TO OPEN THE BASKET OF THE SUBJECT DEVICE, THE HANDLE MOVED BUT THE BASKET DID NOT MOVE AND COULD NOT BE CLOSED. THE PROCEDURE WAS COMPLETED BY COLLECTING THE BASKET AND REPLACING IT WITH ANOTHER PRODUCT. THERE WAS NO EFFECT ON THE PATIENT DUE TO THE EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15245637 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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