Integra® Jarit® 600305Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10381780129400), received between Jan 31, 2023 and Apr 5, 2023 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Overheating of Device” (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.

Most reported problems

Recent adverse event reports

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

• MalfunctionApr 5, 2023Overheating of Device; Overheating of Device

  THIS IS 2 OF 2 REPORTS AND IS RELATED TO MFG REPORT NUMBER 3014334038-2023-00043: IT WAS REPORTED THAT THE INSULATION OF THE SUCTION COAG W/L-HOOK END INS (600305) WAS ¿MELTING¿ AT THE INSTRUMENT END. IT IS UNKNOWN UNDER WHAT CIRCUMSTANCE THIS EVENT OCCURRED; HOWEVER, NO HARM OR SURGICAL DELAY WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16684105 ↗
• MalfunctionApr 5, 2023Overheating of Device; Overheating of Device

  THIS IS 1 OF 2 REPORTS AND IS RELATED TO MFG REPORT NUMBER# 3014334038-2023-00039. IT WAS REPORTED THAT THE INSULATION OF THE SUCTION COAG W/L-HOOK END INS (600305) WAS ¿MELTING¿ AT THE INSTRUMENT END. IT IS UNKNOWN UNDER WHAT CIRCUMSTANCE THIS EVENT OCCURRED; HOWEVER, NO HARM OR SURGICAL DELAY WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16683447 ↗
• MalfunctionJan 31, 2023Sparking; Sparking

  N/A.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16273659 ↗