Integra® Jarit® 100262Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10381780432517), received between Feb 9, 2022 and Jul 10, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (2 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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 10, 2026Break

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25779680 ↗
• MalfunctionFeb 9, 2022Break; Mechanical Problem; Break; Mechanical Problem

  A FACILITY REPORTED THAT THE CURVED METZENBAUM SUPERCUT SCISSOR (102122) BROKE DURING A CASE FOR KNEE ARTHROSCOPY WITH MULTIPLE LIGAMENT REPAIRS WITH ALLOGRAFTS. WHILE CUTTING SOFT TISSUE, THE SHAFT OF THE HANDLE NEAR THE LOCKBOX BROKE AND FLEW BACK, AND NEARLY HIT THE SURGEON IN THE FACE. THE STAFF IRRIGATED HEAVILY TO MAKE SURE ALL SMALL PIECES WERE REMOVED. IT WAS REPORTED THAT NO PART OF THE INSTRUMENT FELL INTO THE SURGICAL SITE THAT COULD BE SEEN WITH THE NORMAL EYE. AN X-RAY WAS PERFORMED MULTIPLE TIMES. THERE WAS A SURGICAL DELAY OF 30 MINUTES, AS THE STAFF HAD TO STOP TO ADDRESS THE ISSUE. THE NURSE OBTAINED ANOTHER PAIR OF METZENBAUM SCISSOR. IT WAS REPORTED THAT THE PATIENT'S OUTCOME WAS GREAT, ALTHOUGH PATIENT HAD TO ENDURE EXTRA MINUTES OF ANESTHESIA AND MORE DOSES OF RADIATION THAT WAS PLANNED FOR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13498296 ↗