Integra® Jarit® 250260Recalls & reported problems
Integra Lifesciences Production Corporation · Integra® Jarit® Lambotte Osteotome, 9", Curved, 6mm Wide · Class 1
- 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 10381780384083), received between Jun 10, 2026 and Jun 10, 2026 — classified as 1 malfunction.
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.
Reports received per month
Most reported problems
Device problems
- Break1
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.
MalfunctionJun 10, 2026Break
THE FOLLOWING WAS REPORTED VIA MEDWATCH/MDR REPORT # MW:5188148: "DURING A TOTAL HIP REVISION, WHILE ATTEMPTING TO TAKE OUT LINER USING A 1/4 OSTEOTOME, THE OSTEOTOME BROKEN HALF." IT IS UNKNOWN WHETHER PATIENT INJURY OR SURGICAL DELAY OCCURRED; HOWEVER, IT WAS MENTIONED THAT THE FAILURE REQUIRED AN INTERVENTION, AND THE SPECIFICITY OF THE INTERVENTION WAS NOT MENTIONED. NO INITIAL REPORTER DETAILS WERE PROVIDED; THUS, NO REQUEST FOR ADDITIONAL INFORMATION IS POSSIBLE AT THIS TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25460678 ↗
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.