Snowden-Pencer 32-5950Recalls & reported problems
Steris Corporation · Snowden-Pencer Plastics DIAMOND-SEREDGES SCISSORS TEBBETTSDELICATE DISSECTING SERRATED, 13,5CM 5-1/4 inches, CURVED · Class 1
All models of Snowden-Pencer (62)
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 10885403148576), received between Dec 23, 2025 and Dec 23, 2025 — 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.
Reports received per month
Most reported problems
Device problems
- Break1
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.
MalfunctionDec 23, 2025Break; Break
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THE TIP OF THEIR TEBBETTS DISSECT SCISSORS BROKE. THE PROCEDURE WAS COMPLETED SUCCESSFULLY USING A DIFFERENT DEVICE. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23881542 ↗
Other SCISSORS, GENERAL, SURGICAL devices
- MEDLINE DYNJ04049Medline Industries, Inc. · SCISSORS, GENERAL, SURGICAL3 recalls2 reports
- MEDLINE DYND04000Medline Industries, Inc. · SCISSORS, GENERAL, SURGICAL3 recalls0 reports
- Centurion 66155Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall1 report
- Sklar Instruments 96-1220Sklar Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Sklar Instruments 96-2503ASklar Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Sklar Instruments 96-2521ASklar Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Centurion I68790Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Sklar Instruments 96-2531Sklar Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
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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