SonoSurg Scissors 5mm O.D.,non HF Series T3075Recalls & 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 04953170208522), received between Nov 22, 2021 and Nov 22, 2021 — 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
- Defective Device1
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.
MalfunctionNov 22, 2021Break; Defective Device; Break; Defective Device
AS REPORTED THE PROBE OF THE SONOSURG SCISSORS IS DEFECTIVE. DURING INTERMEDIATE CLEANING, THE PROBE BROKE OFF OUTSIDE OF THE PATIENT (ABDOMINAL CAVITY). THE DEVICE WAS REPLACED WITH SAME SIMILAR DEVICE AND THE INTENDED PROCEDURE WAS COMPLETED WITHOUT ANY INJURY OR HARM TO THE PATIENT. THERE IS NO USER INJURY ASSOCIATED ON THIS REPORTED EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12853438 ↗
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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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