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DISPOSABLE GRASPING FORCEPS FG-52D (UDI 04953170060595)Recalls & reported problems

Olympus Medical Systems Corp. · Class 2

All models of DISPOSABLE GRASPING FORCEPS (7)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04953170060595), received between Sep 9, 2022 and Sep 9, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Activation Failure” (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

Device problems

  • Activation Failure1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 9, 2022Activation Failure; Activation Failure

    THE CUSTOMER REPORTED THAT THE BASKET DID NOT OPEN WHEN EXTENDED FROM THE FORCEPS CHANNEL DURING AN UNSPECIFIED PROCEDURE. ADJUSTING THE ANGULATION OF THE SCOPE DID NOT RESULT IN THE BASKET OPENING. THE PROCEDURE WAS COMPLETED WITH ANOTHER SIMILAR DEVICE. THERE WAS NO EFFECT ON THE PATIENT DUE TO THE EVENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15393360 ↗

Other Bronchoscope (flexible or rigid) devices

All Bronchoscope (flexible or rigid) devices →

Sources and updates

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