Symmetry Kaye 32-698Recalls & reported problems
Aspen Surgical Products, Inc. · Symmetry® Scissors, Kaye, Curved, Serrated, 5 7/8 in · Class 1
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 00887482071298), received between Jun 16, 2023 and Jun 16, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Fragmentation” (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
- Material Fragmentation1
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.
MalfunctionJun 16, 2023Material Fragmentation; Material Fragmentation
THE CUSTOMER ALLEGED THAT DURING A PLASTIC SURGERY CASE, THE PIECE OF BROKEN TIP FELL INSIDE OF THE PATIENT. THE PIECE WAS RECOVERED WITHOUT ISSUES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17148575 ↗
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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