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Integra® Jarit® 600300Recalls & reported problems

Integra Lifesciences Production Corporation · Integra® Jarit® Suction Coagulator, 13", Spatula Tip, Monopolar control valve, insulated, 5mm · Class 2

All models of Integra Jarit (57)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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 10381780129394), received between Jan 31, 2023 and Jan 31, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Sparking” (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

  • Sparking1

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.

  • MalfunctionJan 31, 2023Sparking; Sparking

    A FACILITY REPORTED THAT THE SUCTION COAG W/SPAT-TIP INS (600300) WAS SPARKING AT END OF INSULATION AND FAILING INSULATION INSPECTIONS. IT WAS REPORTED THAT THE INSTRUMENT WAS NOT USED DURING A PROCEDURE; THUS, NO PATIENT INJURY, DEATH OR SURGICAL DELAY OCCURRED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16274793 ↗

Other COAGULATOR-CUTTER, ENDOSCOPIC, UNIPOLAR (AND ACCESSORIES) devices

All COAGULATOR-CUTTER, ENDOSCOPIC, UNIPOLAR (AND ACCESSORIES) devices →

Sources and updates

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