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DJO SURGICAL 336-02-106Recalls & reported problems

Encore Medical, L.P. · FK 4/3D DOWN 6 POROUS STEMMED, TIBIA, RT · 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 00888912115841), received between Aug 30, 2017 and Aug 30, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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

  • Fracture1

Patient problems

  • Bone Fracture(s)1

Recent adverse event reports

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

  • InjuryAug 30, 2017Fracture

    REVISION SURGERY - DUE TO THE PATIENT HAVING A FRACTURED TIBIA. THE SURGEON DID NOT TELL THE REPRESENTATIVE HOW THE PATIENT FRACTURED THEMSELVES. THE PATELLA WAS THE ONLY IMPLANT LEFT IN PATIENT AND NO OTHER DJO IMPLANT WAS PUT IN.

    Patient problems: Bone Fracture(s)

    MAUDE report 6832650 ↗

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