Skip to content

DJO SURGICAL 335-02-112Recalls & reported problems

Encore Medical, L.P. · TIBIA, STEMMED, POROUS SIZE12 R 3D · Class 2 · Implant

Data updated Oct 18, 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 00888912115759), received between Jun 5, 2018 and Jun 5, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).

5 other recalls cover devices cleared under the same FDA submission (K020114); 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

Device problems

  • Insufficient Device Problem Information1

Patient problems

  • Discomfort1

Recent adverse event reports

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

  • InjuryJun 5, 2018Insufficient Device Problem Information

    REVISION SURGERY - DUE TO THE PATIENT HAVING DISCOMFORT AND THE KNEE WAS VALGUS.

    Patient problems: Discomfort

    MAUDE report 7571261 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K020114. One submission often covers many models, so check the product and lot details in each record.

  • Z-2244-2010 · Jun 28, 2010 · Terminated
    3DKnee Baseplates, Size 8, Left, Part # 333-01-108, Lot# A1000003.
  • Z-1433-2010 · Mar 19, 2010 · Terminated
    3DKNEE SYSTEM, 3D Knee Tibial Insert-DCM, Sterile, Right, size 4 x 11mm. Encore Medical, LP. Austin, TX 78758-5445. Intended to aid the surgion in relieving the patient of knee
  • Z-1539-2008 · Feb 20, 2008 · Terminated
    3DKNEE Tibial Insert Trial, Size 2, 13mm Right; Part #801-01-640; manufactured by Encore Medical, L.P., Austin, TX 78758. Used in surgery to determine the correct size of 3DKnee
  • Z-0332-06 · Nov 3, 2005 · Terminated
    Size 8 right 3DKnee Non-porous Baseplates (Catalog #333-02-108) joint knee replacement.
  • Z-1011-04 · May 10, 2004 · Terminated
    3DKnee System, Stemmed Tibia-Nonporous-3D, Size 6, Right, sterile. Manufactured by Encore Orthopeadics, 9800 Metric Blvd., Austin, Texas 78758

Other PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER devices

All PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page