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Tornier Latitude 9030220Recalls & reported problems

Tornier, Inc. · BELLSAW · Class 1

All models of Tornier Latitude (7)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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 00846832016778), received between Feb 16, 2022 and Feb 16, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Mechanical Jam” (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 18, 2026.

Most reported problems

Device problems

  • Mechanical Jam1

Patient problems

  • Insufficient Information1

Recent adverse event reports

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

  • 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 13546465 ↗

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Sources and updates

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