SonoSurg Straight Scissors,HF,Pistol Grip,5mm x 34cm T3900Recalls & reported problems
Olympus Medical Systems Corp. · Class U
Data updated Oct 18, 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 04953170234941), received between Aug 15, 2019 and Aug 15, 2019 — 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 18, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 15, 2019Break; Break
THE SERVICE CENTER WAS INFORMED THAT DURING A THERAPEUTIC APPENDECTOMY PROCEDURE, THE PROBE TIP BROKE OFF AND FELL INSIDE THE PATIENT. THE DEVICE FRAGMENTS WERE RETRIEVED FROM THE PATIENT. THERE WAS NO REPORT OF BLEEDING. THE INTENDED PROCEDURE WAS COMPLETED WITH A SIMILAR DEVICE. NO OTHER EQUIPMENT WAS REPLACED DURING THE PROCEDURE. THERE WAS NO PATIENT INJURY REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8896328 ↗
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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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