DJO SURGICAL 392-11-705Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00888912120524), received between Feb 11, 2016 and Aug 23, 2023 — classified as 5 injuries.

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

4 other recalls cover devices cleared under the same FDA submission (K091956); 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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• InjuryAug 23, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  REVISION SURGERY DUE TO LOOSENING.

  Patient problems: Joint Laxity

  MAUDE report 17608681 ↗
• InjuryAug 20, 2021Appropriate Device Problem Term/Code Not Available

  REVISION SURGERY - DUE TO INSTABILITY.

  Patient problems: Insufficient Information

  MAUDE report 12350645 ↗
• InjuryJul 9, 2021Appropriate Device Problem Term/Code Not Available

  REVISION SURGERY - PATELLA TENDON RUPTURE. 3D INSERT SWAP.

  Patient problems: Rupture

  MAUDE report 12144240 ↗
• InjurySep 6, 2018Unstable

  REVISION SURGERY - DUE TO THE PATIENT'S KNEE BEING UNSTABLE. THE SURGEON REPLACED THE POLY WITH A THICKER ONE.

  Patient problems: No Code Available

  MAUDE report 7852397 ↗
• InjuryFeb 11, 2016Insufficient Device Problem Information

  REVISION SURGERY - DUE TO THE PATIENT PRESENTING WITH POOR RANGE OF MOTION POST-OPERATIVELY. THE SURGEON DECIDED TO GO BACK WITH A THINNER INSERT.

  Patient problems: Loss of Range of Motion

  MAUDE report 5430828 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K091956. One submission often covers many models, so check the product and lot details in each record.

• Z-2659-2017 · May 31, 2017 · Terminated
  3DKNEE(TM) SYSTEM e+, Tibial Insert, RIGHT Sz 8 / 11mm, REF 391-11-708, QTY 01 The 3DKnee Insert HXL Tibial Inserts are manufactured from ultra high molecular weight polyethylene
• Z-2658-2017 · May 31, 2017 · Terminated
  3DKNEE(TM) SYSTEM e+, tibial Insert, LEFT Sz 6 / 11mm, REF 391-11-706, QTY 01, The 3DKnee Insert HXL Tibial Inserts are manufactured from ultra high molecular weight polyethylene
• Z-1213-2013 · Apr 1, 2013 · Terminated
  3DKnee e+ Tibial Insert. The insert is used along with the other components that comprise the 3DKnee System.
• Z-2302-2012 · Aug 9, 2012 · Terminated
  3DKnee e+ Tibial Insert - HXLPE-VE, Sterile, Material: Highly cross linked vitamin E PE, Sz 2/9mm. The insert is intended to more closely match the kinematics of the knee, allowin