Integra® Jarit® 275525Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10381780385110), received between May 25, 2021 and Nov 13, 2024 — classified as 2 malfunctions.

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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 13, 2024Break; Break

  N/A.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20678124 ↗
• MalfunctionMay 25, 2021Material Fragmentation; Material Fragmentation

  A CUSTOMER REPORTED THAT THE JAW OF THE WIRE CUTTER BROKE DURING AN UNSPECIFIED PROCEDURE AND THE FRAGMENTS FELL INTO THE PATIENT'S BODY. THERE WAS A DELAY IN SURGERY TO FIND THE FRAGMENTS. ALL THE BROKEN PIECES WERE REMOVED AND THE SURGERY WENT WELL. THE EVENT OCCURRED BEFORE (B)(6) 2021; THE EXACT DATE IS UNKNOWN. THE DOCTORS MONITORED THE PATIENT'S CONDITION POST-SURGERY IN CASE SMALL INVISIBLE PIECES REMAINED IN THE BODY, POTENTIALLY CAUSING INFLAMMATION OR OTHER PROBLEMS. ADDITIONAL INFORMATION WAS REQUESTED, BUT HAS NOT BEEN FORTHCOMING.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11878505 ↗