Integra® Miltex® 30-1495Recalls & reported problems
Integra Lifesciences Production Corporation · Integra® Miltex® Tischler Uterine Biopsy Forceps 8-1/2" Shaft, 3mm x 7mm Bite, Shaft Only · 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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10381780428206), received between Sep 9, 2022 and Sep 9, 2022 — classified as 1 injury.
The most frequently reported specific device problem is “Mechanical Problem” (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.
Most reported problems
Device problems
- Mechanical Problem1
Patient problems
- Discomfort1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 9, 2022Mechanical Problem; Mechanical Problem
A FACILITY REPORTED THAT WHILE OBTAINING A VAGINAL TISSUE SAMPLE DURING A WELL WOMEN EXAM, THE CLAMP/TISCHLER - SHAFT ONLY (30-1495) WOULD NOT RELEASE AND INJURED THE PATIENT. AS A RESULT, THE PATIENT EXPERIENCED DISCOMFORT AND BLEEDING. THE EXAM WAS COMPLETED WITHOUT SIGNIFICANT DELAY.
Patient problems: Discomfort
MAUDE report 15396922 ↗
Other FORCEPS, BIOPSY, GYNECOLOGICAL devices
- Trinity Sterile, Inc. 96-4137MTrinity Sterile, Inc. · FORCEPS, BIOPSY, GYNECOLOGICAL1 recall0 reports
- AESCULAP ER063RAesculap AG · FORCEPS, BIOPSY, GYNECOLOGICAL2 reports
- AESCULAP ER064RAesculap AG · FORCEPS, BIOPSY, GYNECOLOGICAL1 report
- Kevorkian-Pacific biopsy punch 64-675Coopersurgical, Inc. · Forceps, Biopsy, Gynecological1 report
- Cervical Biopsy Punch 1Dtr Medical Limited · Forceps, Biopsy, Gynecological1 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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