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Integra® Jarit® 625090HRecalls & reported problems

Integra Lifesciences Production Corporation · Integra® Jarit® Handle/Shaft, 12", Jarit Detach®, Roto-Lok™, monopolar, 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 10381780151777), received between Nov 15, 2022 and Nov 15, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fitting Problem” (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

  • Fitting Problem1

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.

  • MalfunctionNov 15, 2022Fitting Problem; Fitting Problem

    N/A.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15801224 ↗

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Sources and updates

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