Integra® Jarit® 400180Recalls & reported problems
Integra Lifesciences Production Corporation · Integra® Jarit® Knight Nasal Scissors, 6-1/4", 33mm Blade Length · Class 1
- 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 10381780158325), received between Mar 3, 2026 and Mar 3, 2026 — 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. How this data works · Data updated Oct 13, 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.
MalfunctionMar 3, 2026Break
A FACILITY REPORTED THAT DURING A SEPTOPLASTY AND TURBINECTOMY SURGERY, WHILE USING THE PRODUCT KNIGHT NASAL SCS 7 (400180) FOR THE FIRST TIME, THE SCISSORS SNAPPED IN HALF AT THE HANDLE. ALL BROKEN PARTS WERE RECOVERED AND REMOVED USING A GRASPER. THERE WAS A TWO TO THREE MINUTE DELAY WHILE RETRIEVING AND REPLACING THE BROKEN SCISSORS. THERE WAS NO PATIENT INJURY OR DEATH, AND THE PATIENT WAS UNDER ANESTHESIA WHEN THE BREAK OCCURRED. THE PROCEDURE WAS SUCCESSFULLY COMPLETED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24495772 ↗
Other SCISSORS, NASAL devices
- Symmetry Gorney 67-5515Aspen Surgical Products, Inc. · Scissors, Nasal1 report
- V. Mueller RH1634Steris Corporation · SCISSORS, NASAL1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.