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 · TerminatedXP-XP Tibial Tray - Interlok 67 mm Item # 195753
- Z-2523-2019 · Aug 15, 2019 · TerminatedXP-XP Tibial Tray - Interlok 69 mm Item # 195754
- Z-2517-2019 · Aug 15, 2019 · TerminatedXP-XP Tibial Tray - Interlok 87 mm Item # 195760
- Z-2510-2019 · Aug 15, 2019 · TerminatedXP-CR Tibial Tray - Interlok 75mm Item # 195275
- Z-2506-2019 · Aug 15, 2019 · TerminatedXP-CR Tibial Tray - Interlok 67mm Item # 195271
- Z-2508-2019 · Aug 15, 2019 · TerminatedXP-CR Tibial Tray - Interlok 71mm Item # 195273
- Z-2516-2019 · Aug 15, 2019 · TerminatedXP-XP Tibial Tray - Interlok 91mm Item # 195761
- Z-2526-2019 · Aug 15, 2019 · TerminatedXP-XP Tibial Tray - Interlok 63 mm Item # 195751
- Z-2514-2019 · Aug 15, 2019 · TerminatedXP-CR Tibial Tray - Interlok 91 mm Item # 195279
- Z-2522-2019 · Aug 15, 2019 · TerminatedXP-XP Tibial Tray - Interlok 71 mm Item # 195755
- Z-2512-2019 · Aug 15, 2019 · TerminatedXP-CR Tibial Tray - Interlok 83 mm Item # 195277
- Z-2513-2019 · Aug 15, 2019 · TerminatedXP-CR Tibial Tray - Interlok 87 mm Item # 195278
- Z-2504-2019 · Aug 15, 2019 · TerminatedXP-CR Tibial Tray - Interlok 63mm Item # 195269
- Z-2505-2019 · Aug 15, 2019 · TerminatedXP-CR Tibial Tray - Interlok 65mm Item # 195270
- Z-2519-2019 · Aug 15, 2019 · TerminatedXP-XP Tibial Tray - Interlok 79 mm Item # 195758
…and 7 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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