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Vanguard® Knee System 189048Recalls & reported problems

Biomet Orthopedics, LLC · Class 2 · Implant

Data updated Oct 13, 2026 from official FDA records · Editorial policy

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

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier.

10 other recalls cover devices cleared under the same FDA submission (K050222, K113550, K171054); 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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Apr 17, 2020Terminated

    Potential presence of elevated endotoxin levels that exceed the specification limit

    Z-2150-2020 · Root cause: Process control · FDA record ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K050222, K113550, K171054. One submission often covers many models, so check the product and lot details in each record.

  • Z-1607-2024 · Mar 13, 2024 · Open, Classified
    Vanguard Knee System AS Tibial Bearing / DCM ArCom, 12 MM X 75 MM; Model Number 189082. The product is placed into a foil pouch with protective packaging in the form of a polyureth
  • Z-1043-2023 · Dec 29, 2022 · Open, Classified
    (1) Vanguard Knee System PS Open Box Femoral; Left; 57.5 mm. Intended for Knee joint replacement prostheses. Item Number: 183122 EXPANDED RECALL: (2) Vanguard Knee System PS Ope
  • Z-1042-2023 · Dec 29, 2022 · Open, Classified
    (1) Vanguard Knee System PS Open Box Femoral; Right; 60 mm. Intended for knee joint replacement prostheses. Item Number: 183104 (2) Vanguard Knee System PS Open Box Femoral; Right
  • Z-0938-2019 · Dec 21, 2018 · Terminated
    Vanguard Knee System Series-A Standard Patella sizes 34mm Item Number: 184766
  • Z-0495-2019 · Oct 22, 2018 · Terminated
    Vanguard Knee System -PS Open Box Femoral Left, 62.5 mm Item Number: 183126
  • Z-0496-2019 · Oct 22, 2018 · Terminated
    Vanguard Knee System -PS Open Box Femoral Right, 65 mm Item Number:183108
  • Z-2289-2018 · May 24, 2018 · Terminated
    Vanguard Complete Knee System; E1 Vanguard PS Tibial Bearing; Model Numbers EP-183664, EP-183642 Product Usage: The product is intended for use in knee joint replacement arthropla
  • Z-2177-2018 · May 18, 2018 · Terminated
    Biomet Modular Primary Tibial Tray Implants; Modular Interlok Primary Tray (size 75 mm); Item No. 141215; UDI: (01) 00880304005310 (17) 280306 (10) 385340 Product is used in Total
  • Z-2183-2018 · May 11, 2018 · Terminated
    Vanguard Knee System PS Tibial Bearing, Part Number 183621 Intended for use in knee joint replacement procedures.
  • Z-1011-2018 · Oct 3, 2017 · Terminated
    Vanguard CR Porous Femoral 62.5mm (Left Femur) For use in total knee arthroplasty

Other PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER devices

All PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER devices →

Sources and updates

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