Skip to content

LEGION 71453241Recalls & reported problems

Smith & Nephew, Inc. · LEGION HIGHLY CROSS LINKED POLYETHYLENE POSTERIOR STABILIZED INSERT SIZE 1-2 9MM · Class 2 · Implant

All models of LEGION (446)

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

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00885556255957), received between Dec 30, 2019 and Dec 7, 2021 — classified as 2 injuries.

The most frequently reported specific device problem is “Break” (1 report).

6 other recalls cover devices cleared under the same FDA submission (K071071, K230653); they may or may not involve this specific model.

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

  • Adverse Event Without Identified Device or Use Problem1
  • Break1

Patient problems

  • Injury1
  • Loss of Range of Motion1
  • Pain1

Recent adverse event reports

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

  • InjuryDec 7, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT PHYSICIAN WANTS TO TAKE THE LGN XLPE PS INSERT SZ 1-2 9MM OUT SINCE THE KNEE HAS NO RANGE OF MOTION. IT IS UNKNOWN IF IT HAS BEEN SOLVED OR NOT. PATIENT OUTCOME IS UNKNOWN.

    Patient problems: Loss of Range of Motion; Pain

    MAUDE report 12953777 ↗
  • InjuryDec 30, 2019Break; Break

    IT WAS REPORTED THAT REVISION SURGERY WAS PERFORMED DUE TO BREAKAGE OF THE PS LINER.

    Patient problems: Injury

    MAUDE report 9530473 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K071071, K230653. One submission often covers many models, so check the product and lot details in each record.

  • Z-2621-2023 · Aug 31, 2023 · Open, Classified
    smith&nephew LEGION OXINUM POSTERIOR STABILIZED NONPOROUS FERMOAL COMPONENT, SIZE 5N, LEFT, NARROW, REF 71421265; knee joint
  • Z-1507-2020 · Dec 19, 2019 · Terminated
    LEGION PS High Flex XLPE size 5-6 9mm Articular Insert
  • Z-1907-2018 · Mar 30, 2018 · Terminated
    smith&nephew LEGION(R) CR XLPE HIGH LEXION Articular Insert, 1-2 Size, 9 MM, REF 71453101designed for use in patients in primary and revision surgery, where the anterior and poster
  • Z-1906-2018 · Mar 30, 2018 · Terminated
    smith&nephew LEGION(R) CR XLPE HIGH LEXION Articular Insert, 5-6 Size, 9 MM, REF 71453121 designed for use in patients in primary and revision surgery, where the anterior and poste
  • Z-1904-2018 · Mar 30, 2018 · Terminated
    smith&nephew LEGION(R) CR XLPE HIGH LEXION Articular Insert, 5-6 Size, 10 MM, REF 71453185 designed for use in patients in primary and revision surgery, where the anterior and post
  • Z-1905-2018 · Mar 30, 2018 · Terminated
    smith&nephew LEGION(R) CR XLPE HIGH LEXION Articular Insert, 5-6 Size, 11 MM, REF 71453122 designed for use in patients in primary and revision surgery, where the anterior and post

Other PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER devices

All PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page