Tornier Latitude 9030200Recalls & reported problems
Tornier, Inc. · ULNAR JIG · Class 1
All models of Tornier Latitude (7)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00846832015160), received between Feb 16, 2022 and May 27, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Mechanical Jam” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Mechanical Jam2
Patient problems
- Insufficient Information2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 27, 2025Mechanical Jam; Mechanical Jam
DURING PRIMARY RIGHT TOTAL ELBOW REPLACEMENT, SEVERAL ISSUES AROSE REGARDING LATITUDE EV INSTRUMENT MALFUNCTION. 1. DURING INITIAL PREPARATION OF THE ULNAR, THE ULNAR JIG, RIGHT WAS FITTED IN PLACE AS PER THE SURGICAL TECHNIQUE. THE LARGE SIZING HUMERAL SPOOL WAS SLID OVER THE CENTRAL AXEL OF THE JIG, AND THE LARGE BELLSAW WAS THEN PLACED OVER THE SPOOL, IN PREPARATION FOR PROFILING THE PROXIMAL ULNAR. WHEN THE SURGEON ACTIVATED THE DRILL-REAMER POWER TOOL, THE BELL SAW CENTRAL AXEL JAMMED WITHIN THE HOLLOW CENTRAL AXEL OF THE JIG. THE SURGEON WAS UNABLE TO ADVANCE THE BELLSAW, OR REMOVE IT, AS IT APPEARED THAT THE METAL SURFACES HAD JAMMED TOGETHER. THE JIG WAS FULLY LOOSENED, THE BELLSAW DETACHED FROM THE DRILL / REAMER POWER TOOL, AND THE JAMMED CONSTRUCT WAS REMOVED, CAREFULLY, FROM THE ELBOW JOINT. THE BELLSAW WAS THEN ABLE TO BE DETACHED FROM THE JIG. ON INSPECTION, THE INNER HOLLOW TUBE OF THE ULNAR JIG, RIGHT, APPEARED TO HAVE METAL FATIGUE, CAUSING THE CENTRAL AXEL OF THE BELLSAW TO JAM. THE SURGEON DECIDED TO USE THE ULNAR JIG, LEFT, FLIPPED IT OVER, POSITIONED IT IN PLACE, AND COMPLETED THE PROFILING OF THE PROXIMAL ULNAR, TO HIS SATISFACTION. NO FURTHER ISSUES WITH USIN
Patient problems: Insufficient Information
MAUDE report 22086850 ↗MalfunctionFeb 16, 2022Mechanical Jam; Mechanical Jam
IT WAS REPORTED THAT THE ULNAR REAMER GOT STUCK AND WOULDN'T WORK.
Patient problems: Insufficient Information
MAUDE report 13546462 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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