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VANGUARD COMPLETE KNEE SYSTEM 195557Recalls & reported problems

Biomet Orthopedics, LLC · Class 2 · Implant

All models of Vanguard Complete Knee System (27)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00880304558618), received between Feb 18, 2020 and Feb 18, 2020 — classified as 1 injury.

22 other recalls cover devices cleared under the same FDA submission (K132873); 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 16, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Adhesion(s)1
  • Limited Mobility Of The Implanted Joint1
  • Scar Tissue1

Recent adverse event reports

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

  • InjuryFeb 18, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

    Patient problems: Adhesion(s); Limited Mobility Of The Implanted Joint; Scar Tissue

    MAUDE report 9722477 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K132873. One submission often covers many models, so check the product and lot details in each record.

  • Z-2524-2019 · Aug 15, 2019 · Terminated
    XP-XP Tibial Tray - Interlok 67 mm Item # 195753
  • Z-2523-2019 · Aug 15, 2019 · Terminated
    XP-XP Tibial Tray - Interlok 69 mm Item # 195754
  • Z-2517-2019 · Aug 15, 2019 · Terminated
    XP-XP Tibial Tray - Interlok 87 mm Item # 195760
  • Z-2510-2019 · Aug 15, 2019 · Terminated
    XP-CR Tibial Tray - Interlok 75mm Item # 195275
  • Z-2506-2019 · Aug 15, 2019 · Terminated
    XP-CR Tibial Tray - Interlok 67mm Item # 195271
  • Z-2508-2019 · Aug 15, 2019 · Terminated
    XP-CR Tibial Tray - Interlok 71mm Item # 195273
  • Z-2516-2019 · Aug 15, 2019 · Terminated
    XP-XP Tibial Tray - Interlok 91mm Item # 195761
  • Z-2526-2019 · Aug 15, 2019 · Terminated
    XP-XP Tibial Tray - Interlok 63 mm Item # 195751
  • Z-2514-2019 · Aug 15, 2019 · Terminated
    XP-CR Tibial Tray - Interlok 91 mm Item # 195279
  • Z-2522-2019 · Aug 15, 2019 · Terminated
    XP-XP Tibial Tray - Interlok 71 mm Item # 195755
  • Z-2512-2019 · Aug 15, 2019 · Terminated
    XP-CR Tibial Tray - Interlok 83 mm Item # 195277
  • Z-2513-2019 · Aug 15, 2019 · Terminated
    XP-CR Tibial Tray - Interlok 87 mm Item # 195278
  • Z-2504-2019 · Aug 15, 2019 · Terminated
    XP-CR Tibial Tray - Interlok 63mm Item # 195269
  • Z-2505-2019 · Aug 15, 2019 · Terminated
    XP-CR Tibial Tray - Interlok 65mm Item # 195270
  • Z-2519-2019 · Aug 15, 2019 · Terminated
    XP-XP Tibial Tray - Interlok 79 mm Item # 195758

…and 7 more.

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