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LEGION 71434334Recalls & reported problems

Smith & Nephew, Inc. · LEGION TIBIAL DRILL GUIDE SIZE 1 · Class 2

All models of LEGION (446)

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 03596010549846), received between Sep 28, 2021 and Dec 20, 2021 — classified as 2 malfunctions.

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

Most reported problems

Device problems

  • Break2

Patient problems

  • No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

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

  • MalfunctionDec 20, 2021Break; Break

    IT WAS REPORTED THAT A LEGION TIBIAL DRILL GUIDE SIZE 1 IS BROKEN. THE CONTEXT IN WHICH THIS OBSERVATION WAS MADE IS UNSPECIFIED. THEREFORE, PATIENT INVOLVEMENT IS YET TO BE CONFIRMED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13047792 ↗
  • MalfunctionSep 28, 2021Break; Break

    IT WAS REPORTED DURING A FIELD INSPECTION THAT A LGN TIBIAL DRILL GUIDE SIZE 1 IS BROKEN. NO PATIENT INVOLVED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12538463 ↗

Other PLATE, FIXATION, BONE devices

All PLATE, FIXATION, BONE devices →

Sources and updates

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