DJO SURGICAL 391-09-606Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00888912118866), received between Jun 14, 2017 and Apr 29, 2025 — classified as 6 injuries.

The most frequently reported specific device problem is “Device Inoperable” (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

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• InjuryApr 29, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  REVISION SURGERY - DUE TO POLY SWAP FOR UNKNOWN REASON.

  Patient problems: Insufficient Information

  MAUDE report 21931585 ↗
• InjuryMay 6, 2020Naturally Worn

  REVISION SURGERY - DUE TO EXCESSIVE POLY WEAR.

  Patient problems: No Code Available

  MAUDE report 10030780 ↗
• InjuryJul 11, 2019Appropriate Device Problem Term/Code Not Available

  REVISION SURGERY - PATIENT HAD INFECTION. PERFORMED A WASH OUT AND REPLACED THE INSERT.

  Patient problems: Unspecified Infection

  MAUDE report 8783154 ↗
• InjuryApr 4, 2018Device Inoperable

  REPORTED INCIDENT - DUE TO LEFT KNEE FAILURE, LIMITED RANGE OF MOTION.

  Patient problems: Loss of Range of Motion

  MAUDE report 7397356 ↗
• InjuryDec 6, 2017Unstable

  REVISION SURGERY - DUE TO THE PATIENT'S KNEE BECOMING UNSTABLE.

  Patient problems: No Code Available

  MAUDE report 7086948 ↗
• InjuryJun 14, 2017Appropriate Device Problem Term/Code Not Available

  REVISION SURGERY - THE PATIENT WAS EXPERIENCING PAIN, THE SURGEON SWAPPED TO A LARGE SIZE. THERE WAS NO SIGN OF WEAR.

  Patient problems: Pain

  MAUDE report 6641023 ↗

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