Integra® Miltex® 5-320Recalls & reported problems
Integra Lifesciences Production Corporation · Integra® Miltex® Goldman-Fox Scissors, 5-1/8", Curved, One Serrated Blade · Class 1
All models of Integra Miltex (21)
Data updated Oct 16, 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 10381780501459), received between Jul 2, 2025 and Jul 2, 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 16, 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.
MalfunctionJul 2, 2025Break; Break
A FACILITY REPORTED THAT WHILE USING THE GOLDMAN-FOX WOUND SCISSOR, 5 (100-9837), THE TIP BROKE OFF IN THE PATIENT'S MOUTH. THE FACILITY REPORTED THAT THE PATIENT IS OKAY, AND THERE WAS NO SERIOUS INJURY OR MEDICAL ATTENTION REQUIRED." STAFF WAS ABLE TO GET THE TIP OUT OF THE MOUTH SAFELY AND IT WAS NOT SWALLOWED. THE ITEM WAS DISCARDED BY THE FACILITY. THE TOTAL USES OF THE SCISSOR PRIOR TO BREAKAGE WERE UNKNOWN. NO INJURY, DEATH OR SURGICAL DELAY WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22391717 ↗
Other SCISSORS, GENERAL, SURGICAL devices
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- MEDLINE DYND04000Medline Industries, Inc. · SCISSORS, GENERAL, SURGICAL3 recalls0 reports
- Centurion 66155Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall1 report
- Sklar Instruments 96-2673ASklar Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Sklar Instruments 96-2266Sklar Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Sklar Instruments 96-2502Sklar Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Centurion TRI67630Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Sklar Instruments 96-2492ASklar 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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