Integra® Jarit® 140223Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10381780379300), received between Feb 18, 2025 and Feb 18, 2025 — classified as 1 injury.

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 18, 2025Break; Break

  THE FOLLOWING INFORMATION WAS RECEIVED VIA MDR REPORT# MW5164844: "ONE OF THE RESIDENTS WAS PUTTING IN A SCREW IN THE HIP USED A RIGHT ANGLECLAMP TO MANIPULATE A TISSUE THEN THE TIP OF THE CLAMP BROKE OFF. BOTH DOCTORS TRIED TO FISH OUT THE BROKEN PIECE OF CLAMP FOR MORE THAN 30MIN, COULD NOT FIND THE PIECE THEN DECIDED THAT IT WAS MORE RISK TO TAKE IT OUTTHAN LEAVING IT IN THE PATIENT.¿ IT IS UNKNOWN WHETHER AN X-RAY WAS PERFORMED TO CONFIRM PRESENCE OF FOREIGN BODY. ADDITIONAL INFORMATION HAS BEEN REQUESTED.

  Patient problems: Foreign Body In Patient

  MAUDE report 21402290 ↗