Symmetry Surgical 57-2610Recalls & reported problems
Aspen Surgical Products, Inc. · Symmetry® Scissors, Micro Bayonet, Straight, Serrated Blade, Flat Handle, 9 1/4 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 00887482095379), received between Sep 4, 2018 and Sep 4, 2018 — 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.
MalfunctionSep 4, 2018Break
SCISSOR TIP BROKE DURING SURGICAL PROCEDURE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7844547 ↗
Other Instrument, Microsurgical devices
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- Integra® Ruggles®-Redmond™ RN6202Integra Lifesciences Production Corporation · INSTRUMENT, MICROSURGICAL2 reports
- Integra® Jarit® 277274TIIntegra Lifesciences Production Corporation · INSTRUMENT, MICROSURGICAL1 report
- Avalign VM82-7222Avalign Technologies, Inc. · INSTRUMENT, MICROSURGICAL1 report
- V. Mueller NL3785-009Steris Corporation · INSTRUMENT, MICROSURGICAL1 report
- Integra® Ruggles®-Redmond™ RN6206Integra Lifesciences Production Corporation · INSTRUMENT, MICROSURGICAL1 report
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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