VANGUARD COMPLETE KNEE SYSTEM 195772Recalls & 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 00880304552760), received between Oct 30, 2020 and Oct 30, 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
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 30, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
UPON REASSESSMENT OF THE REPORTED EVENT, IT WAS IDENTIFIED THAT THIS DEVICE DID NOT CAUSE OR CONTRIBUTE TO THE REPORTED EVENT.
Patient problems: Pain
MAUDE report 10763913 ↗
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-2523-2019 · Aug 15, 2019 · TerminatedXP-XP Tibial Tray - Interlok 69 mm Item # 195754
- Z-2524-2019 · Aug 15, 2019 · TerminatedXP-XP Tibial Tray - Interlok 67 mm Item # 195753
- Z-2504-2019 · Aug 15, 2019 · TerminatedXP-CR Tibial Tray - Interlok 63mm Item # 195269
- Z-2513-2019 · Aug 15, 2019 · TerminatedXP-CR Tibial Tray - Interlok 87 mm Item # 195278
- Z-2507-2019 · Aug 15, 2019 · TerminatedXP-CR Tibial Tray - Interlok 69mm Item # 195272
- 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-2522-2019 · Aug 15, 2019 · TerminatedXP-XP Tibial Tray - Interlok 71 mm Item # 195755
- Z-2519-2019 · Aug 15, 2019 · TerminatedXP-XP Tibial Tray - Interlok 79 mm Item # 195758
- Z-2505-2019 · Aug 15, 2019 · TerminatedXP-CR Tibial Tray - Interlok 65mm Item # 195270
- Z-2512-2019 · Aug 15, 2019 · TerminatedXP-CR Tibial Tray - Interlok 83 mm Item # 195277
- Z-2508-2019 · Aug 15, 2019 · TerminatedXP-CR Tibial Tray - Interlok 71mm Item # 195273
- Z-2518-2019 · Aug 15, 2019 · TerminatedXP-XP Tibial Tray - Interlok 83 mm Item # 195759
- Z-2525-2019 · Aug 15, 2019 · TerminatedXP-XP Tibial Tray - Interlok 65 mm Item # 195752
- Z-2520-2019 · Aug 15, 2019 · TerminatedXP-XP Tibial Tray - Interlok 75 mm Item # 195757
…and 7 more.
Other PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER devices
- ATTUNE 1512-14-050Depuy (Ireland) · PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER106 reports
- ATTUNE 1504-40-205Depuy (Ireland) · PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER1 recall53 reports
- ATTUNE 1504-40-105Depuy (Ireland) · PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER1 recall46 reports
- ATTUNE 1547-06-001Depuy (Ireland) · PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER1 recall37 reports
- ATTUNE 1513-12-060Depuy (Ireland) · PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER72 reports
- Triathlon 5531-G-709-EHowmedica Osteonics Corp. · PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER1 recall19 reports
- Triathlon 5521-B-300Howmedica Osteonics Corp. · PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER1 recall19 reports
- Triathlon 5531-G-610-EHowmedica Osteonics Corp. · PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER1 recall16 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.
How reports and recalls are matched · Editorial policy · Report an error on this page