AGC V2 TOTAL KNEE SYSTEM 155033Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05019279390519), received between Mar 30, 2020 and Mar 30, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (1 report).

2 other recalls cover devices cleared under the same FDA submission (K833921); 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 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryMar 30, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT A PATIENT UNDERWENT AN INITIAL LEFT TOTAL HIP ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT UNDERWENT A CLOSED REDUCTION DUE TO DISLOCATION. THE COMPLICATION WAS RESOLVED WITH NO FURTHER ISSUES REPORTED.

  Patient problems: Joint Dislocation

  MAUDE report 9897765 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K833921. One submission often covers many models, so check the product and lot details in each record.

• Z-0628-2018 · Aug 25, 2017 · Terminated
  AGC 2000 LP Patella, labeled as AGC Porous Patellar Med, Model Number 150804. Product Usage: For use in Total Knee Arthroplasty.
• Z-0627-2018 · Aug 25, 2017 · Terminated
  AGC 2000 LP Patella, labeled as AGC Porous Patellar SM, Model Number 150802. Product Usage: For use in Total Knee Arthroplasty.