Integra® Miltex® V930-965Recalls & reported problems
Integra Lifesciences Production Corporation · Integra® Miltex® Schroeder Tenaculum Forceps, 9-3/4", Straight · Class 2
All models of Integra Miltex (21)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10381780177616), received between Jun 22, 2022 and Jun 22, 2022 — classified as 3 injuries.
The most frequently reported specific device problem is “Physical Resistance/Sticking” (3 reports).
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.
Most reported problems
Device problems
- Physical Resistance/Sticking3
Patient problems
- Hemorrhage/Blood Loss/Bleeding3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryJun 22, 2022Physical Resistance/Sticking; Physical Resistance/Sticking
THIS IS 3 OF 3 REPORTS LINKED TO MFG REPORT NUMBERS: 3014334038-2022-00127 AND 3014334038-2022-00128. A FACILITY REPORTED THAT THE VANTAGE SCHROEDER TENACULUM FORCEPS (V930-965) WAS VERY STIFF AND CLAMPED DOWN HARD ON THE PATIENT'S CERVIX CAUSING BLEEDING. IT WAS REPORTED THAT THERE WAS NO ADVERSE CONSEQUENCES TO THE PATIENT FOLLOWING THE EVENT.
Patient problems: Hemorrhage/Blood Loss/Bleeding
MAUDE report 14766165 ↗InjuryJun 22, 2022Physical Resistance/Sticking; Physical Resistance/Sticking
THIS IS 2 OF 3 REPORTS LINKED TO MFG REPORT NUMBERS: 3014334038-2022-00127 AND 3014334038-2022-00129. A FACILITY REPORTED THAT THE VANTAGE SCHROEDER TENACULUM FORCEPS (V930-965) WAS VERY STIFF AND CLAMPED DOWN HARD ON THE PATIENT'S CERVIX CAUSING BLEEDING. IT WAS REPORTED THAT THERE WAS NO ADVERSE CONSEQUENCES TO THE PATIENT FOLLOWING THE EVENT.
Patient problems: Hemorrhage/Blood Loss/Bleeding
MAUDE report 14766164 ↗InjuryJun 22, 2022Physical Resistance/Sticking; Physical Resistance/Sticking
THIS IS 1 OF 3 REPORTS LINKED TO MFG REPORT NUMBERS: 3014334038-2022-00128 AND 3014334038-2022-00129. A FACILITY REPORTED THAT THE VANTAGE SCHROEDER TENACULUM FORCEPS (V930-965) WAS VERY STIFF AND CLAMPED DOWN HARD ON THE PATIENT'S CERVIX CAUSING BLEEDING. IT WAS REPORTED THAT THERE WAS NO ADVERSE CONSEQUENCES TO THE PATIENT FOLLOWING THE EVENT.
Patient problems: Hemorrhage/Blood Loss/Bleeding
MAUDE report 14766159 ↗
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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