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Integra® Jarit® 275510Recalls & reported problems

Integra Lifesciences Production Corporation · Integra® Jarit® Wire Cutter, 7", 1.7mm Maximum, Double-Action, Carb-Edge™, Angled Up · Class 1

Data updated Oct 13, 2026 from official FDA records · Editorial policy

Adverse event reports
3
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10381780385097), received between Dec 16, 2022 and Jan 12, 2026 — classified as 3 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. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 1 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Break2
  • Failure to Cut1
  • Material Frayed1

Patient problems

  • No Clinical Signs, Symptoms or Conditions3

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJan 12, 2026Break

    THE FOLLOWING WAS REPORTED VIA MEDWATCH/MDR REPORT # MW5179561: "DURING A SCHEDULED SURGERY OF LEFT DISTAL RADIUS OPEN REDUCTION INTERNAL FIXATION ON, SURGEON ATTEMPTED TO USE A WIRE CUTTER TO TRIM A METAL WIRE AND UNEXPECTEDLY THEY STATED THAT THE WIRE CUTTER'S BLADE SCATTERED INTO MULTIPLE PIECES AND FELL INTO PATIENT'S SURGICAL SITE." ATTEMPTS HAVE BEEN MADE TO OBTAIN ADDITIONAL INFORMATION REGARDING THE SELECTION CLINICAL CODE: ALTERED STATE OF CONSCIOUS IN VOLUNTARY MEDWATCH REPORT. NO ADDITIONAL INFORMATION HAS BEEN PROVIDED AT THIS TIME.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24036583 ↗
  • MalfunctionMar 2, 2023Failure to Cut; Failure to Cut

    THE WIRE CUTTER WAS USED TO CUT K-WIRE, BUT THE ENDS OF THE K-WIRE FRAYED AND SMALL FRAGMENTS BROKE OFF INTO THE PATIENT DURING SURGERY. THE BROKEN PIECES WERE RECOVERED. NO PATIENT INJURY OCCURRED; HOWEVER, THERE WAS AN UNSPECIFIED DELAY IN SURGERY TIME.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16465747 ↗
  • MalfunctionDec 16, 2022Break; Material Frayed; Break; Material Frayed

    A FACILITY REPORTED THAT THERE WERE INSTANCES USING THE CARB-EDGE D/A WIRE CUTTER 7 (275-510) WHERE THEY WERE CUTTING A K-WIRE AND IT FRAYED AT THE ENDS OF THE K-WIRE OR SMALL FRAGMENTS BROKE OFF INTO THE PATIENT DURING SURGERY. THE BROKEN PIECE WAS RECOVERED. NO PATIENT INJURY OCCURRED; HOWEVER, THERE WAS AN UNSPECIFIED DELAY IN SURGERY TIME.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15996593 ↗

Other CUTTER, WIRE devices

All CUTTER, WIRE devices →

Sources and updates

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