Vanguard® Knee System 183026Recalls & reported problems
Biomet Orthopedics, LLC · Class 2 · Implant
All models of Vanguard Knee System (147)
Data updated Oct 16, 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 00880304270503), received between Mar 5, 2020 and Apr 15, 2020 — classified as 2 injuries.
The most frequently reported specific device problem is “Loss of or Failure to Bond” (1 report).
20 other recalls cover devices cleared under the same FDA submission (K023546, 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Loss of or Failure to Bond1
- Patient Device Interaction Problem1
- Unstable1
Patient problems
- Ambulation or Postural Difficulties1
- Limited Mobility Of The Implanted Joint1
- Loss of Range of Motion1
- Muscular Rigidity1
- Pain1
- Scar Tissue1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryApr 15, 2020Patient Device Interaction Problem; Patient Device Interaction Problem
THE PATIENT UNDERWENT A MANIPULATION UNDER ANESTHESIA APPROXIMATELY 2 MONTHS POST-OP, DUE TO ARTHROFIBROSIS STIFFNESS. THE ISSUE WAS REPORTED TO HAVE RESOLVED ONE WEEK AFTER THE MUA WITHOUT FURTHER COMPLICATION.
Patient problems: Limited Mobility Of The Implanted Joint; Loss of Range of Motion; Muscular Rigidity; Scar Tissue
MAUDE report 9962375 ↗InjuryMar 5, 2020Loss of or Failure to Bond; Unstable; Loss of or Failure to Bond; Unstable
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Ambulation or Postural Difficulties; Pain
MAUDE report 9793729 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K023546, K113550, K171054. One submission often covers many models, so check the product and lot details in each record.
- 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-2153-2020 · Apr 17, 2020 · TerminatedKnee Products: 183742 Vanguard Knee System, PS+ Tibial Bearing, 12 MM, 71/75 MM EP-183608 Vanguard Knee System, PS Tibial Bearing, E1 Infused, 18 MM X 59 MM EP-183608 Vang
- Z-2150-2020 · Apr 17, 2020 · TerminatedKnee Products: 183622 Vanguard Knee System PS Tibial Bearing, 12 MM X 63/67 MM 183620 Vanguard Knee System PS Tibial Bearing, 10 MM X 63/67 MM 189048 Vanguard Knee System, AS Tibia
- Z-0938-2019 · Dec 21, 2018 · TerminatedVanguard Knee System Series-A Standard Patella sizes 34mm Item Number: 184766
- Z-0496-2019 · Oct 22, 2018 · TerminatedVanguard Knee System -PS Open Box Femoral Right, 65 mm Item Number:183108
- Z-0495-2019 · Oct 22, 2018 · TerminatedVanguard Knee System -PS Open Box Femoral Left, 62.5 mm Item Number: 183126
- Z-2289-2018 · May 24, 2018 · TerminatedVanguard 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 · TerminatedBiomet 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 · TerminatedVanguard Knee System PS Tibial Bearing, Part Number 183621 Intended for use in knee joint replacement procedures.
- Z-1011-2018 · Oct 3, 2017 · TerminatedVanguard CR Porous Femoral 62.5mm (Left Femur) For use in total knee arthroplasty
- Z-0674-2018 · Sep 29, 2017 · TerminatedVanguard Complete Knee System, Vanguard CR Lipped Tibial Bearing 10x71/75, Item Number: 183540 Product Usage: For use in total knee arthroplasty
- Z-0673-2018 · Sep 29, 2017 · TerminatedVanguard Complete Knee System, Vanguard CR Tibial Bearing 12x71/75, Item Number: 183442 Product Usage: For use in total knee arthroplasty
- Z-1115-2017 · Jan 4, 2017 · TerminatedVanguard Total Knee System Vanguard Open Box Femoral Components Item Number: 183100 Description: VNGD PS OPEN INTL FEM RT 55 Item Number: 183102 Description: VNGD PS OPEN INTL FEM
- Z-0111-2017 · Aug 9, 2016 · TerminatedVanguard Distal Femoral Augment 75 X 5 RL/LM Product Usage: Painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or
…and 5 more.
Other PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER devices
- ATTUNE 1506-00-005Depuy (Ireland) · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER589 reports
- ATTUNE 1506-00-004Depuy (Ireland) · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER580 reports
- JOURNEY 74012812Smith & Nephew, Inc. · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER502 reports
- JOURNEY 74011856Smith & Nephew, Inc. · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER438 reports
- PERSONA™ 42-5099-094-00Zimmer, Inc. · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER406 reports
- JOURNEY 74011857Smith & Nephew, Inc. · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER388 reports
- ATTUNE 1506-00-007Depuy (Ireland) · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER288 reports
- ATTUNE 1506-00-003Depuy (Ireland) · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER271 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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