VANGUARD COMPLETE KNEE SYSTEM 195756Recalls & 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 00880304552272), received between Oct 23, 2024 and Oct 23, 2024 — 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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 23, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT A MANIPULATION UNDER ANESTHESIA TWO (2) MONTHS FOLLOWING RIGHT KNEE ARTHROPLASTY TO ADDRESS PAIN, STIFFNESS, RESTRICTED RANGE OF MOTION AND CONCERN FOR ARTHROFIBROSIS. HOWEVER, THE PATIENT CONTINUED TO EXPERIENCE LIMITED RANGE OF MOTION AND WAS SUBSEQUENTLY REVISED. DURING THE REVISION, BOTH THE MEDIAL AND LATERAL TIBIAL BEARINGS WERE NOTED TO NOT BE FULLY SEATED AND THE LATERAL TIBIAL BEARING WAS PARTIALLY FRACTURED. ARTHROLYSIS AND DEBRIDEMENT WERE PERFORMED TO REMOVE SCAR TISSUE AND THE TIBIAL BEARINGS AND LOCKING BAR WERE REPLACED. NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: Pain
MAUDE report 20515545 ↗
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-2519-2019 · Aug 15, 2019 · TerminatedXP-XP Tibial Tray - Interlok 79 mm Item # 195758
- Z-2511-2019 · Aug 15, 2019 · TerminatedXP-CR Tibial Tray - Interlok 79 mm Item # 195276
- Z-2516-2019 · Aug 15, 2019 · TerminatedXP-XP Tibial Tray - Interlok 91mm Item # 195761
- Z-2510-2019 · Aug 15, 2019 · TerminatedXP-CR Tibial Tray - Interlok 75mm Item # 195275
- Z-2505-2019 · Aug 15, 2019 · TerminatedXP-CR Tibial Tray - Interlok 65mm Item # 195270
- Z-2509-2019 · Aug 15, 2019 · TerminatedXP-CR Tibial Tray - Interlok 73mm Item # 195274
- 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-2517-2019 · Aug 15, 2019 · TerminatedXP-XP Tibial Tray - Interlok 87 mm Item # 195760
- Z-2522-2019 · Aug 15, 2019 · TerminatedXP-XP Tibial Tray - Interlok 71 mm Item # 195755
- Z-2525-2019 · Aug 15, 2019 · TerminatedXP-XP Tibial Tray - Interlok 65 mm Item # 195752
- Z-2507-2019 · Aug 15, 2019 · TerminatedXP-CR Tibial Tray - Interlok 69mm Item # 195272
- Z-2514-2019 · Aug 15, 2019 · TerminatedXP-CR Tibial Tray - Interlok 91 mm Item # 195279
- Z-2518-2019 · Aug 15, 2019 · TerminatedXP-XP Tibial Tray - Interlok 83 mm Item # 195759
…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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