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
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
- NA 03.607.513Synthes GmbH · CUTTER, WIRE35 reports
- NA 03.221.006Synthes GmbH · CUTTER, WIRE34 reports
- NA 388.72Synthes GmbH · CUTTER, WIRE29 reports
- NA 03.221.008Synthes GmbH · CUTTER, WIRE11 reports
- NA 391.93Synthes GmbH · CUTTER, WIRE9 reports
- NA 391.771Synthes GmbH · CUTTER, WIRE8 reports
- NA 391.906Synthes GmbH · CUTTER, WIRE8 reports
- NA 391.905Synthes GmbH · CUTTER, WIRE7 reports
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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