Skip to content

DJO SURGICAL 311-02-104Recalls & reported problems

Encore Medical, L.P. · BASEPLATE,TIBIAL, STEMMED, POROUS SIZE4 L W/NS BEADS · 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 00888912113687), received between Mar 24, 2016 and Mar 24, 2016 — classified as 1 injury.

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

5 other recalls cover devices cleared under the same FDA submission (K923277, K970031); 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

  • Device Slipped1

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.

  • InjuryMar 24, 2016Device Slipped

    REVISION SURGERY - DUE TO THE PATIENT HAVING RECURRING PAIN; THE SURGEON FELT THE TIBIAL COMPONENT HAD POSSIBLY LOOSENED.

    Patient problems: Pain

    MAUDE report 5522026 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K923277, K970031. One submission often covers many models, so check the product and lot details in each record.

  • Z-0349-2012 · Oct 26, 2011 · Terminated
    Foundation Tibial Broach P/N 801-01-013 Foundation Tibial Broach to be used in conjunction with the Tibial Sizing Template and Tibial Broach Guide to prepare the resected tibial
  • Z-2466-2008 · Aug 4, 2008 · Terminated
    FOUNDATION KNEE SYSTEM Tibial Fixed Impactor, Revision A and B; Catalog #801-01-449; distributed by Encore Medical, L.P., Austin, TX 78758. The Tibial Fixed Impactor, a part of t
  • Z-0331-06 · Nov 3, 2005 · Terminated
    Size 6 right Foundation Total Knee System (Catalog #324-01-106) knee joint replacement.
  • Z-1010-04 · May 10, 2004 · Terminated
    Foundation Knee System, Tibia-Nonporous, Size 6, Right, sterile. Manufactured by Encore Orthopeadics, 9800 Metric Blvd., Austin, Texas 78758
  • Z-1069-03 · Apr 24, 2003 · Terminated
    Foundation Knee System, non-porous Femur Size 8, Right

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