Skip to content

DJO SURGICAL 233-02-105Recalls & reported problems

Encore Medical, L.P. · FEMUR, NONPOROUS, 3D, SIZE5, RT · Class 2 · Implant

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00888912111225), received between Jan 12, 2018 and Oct 3, 2022 — classified as 2 injuries.

The most frequently reported specific device problem is “Loose or Intermittent Connection” (1 report).

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

  • Adverse Event Without Identified Device or Use Problem1
  • Loose or Intermittent Connection1

Patient problems

  • Joint Laxity1
  • No Code Available1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryOct 3, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    REVISION SURGERY - KNEE INSTABILITY DUE TO LOOSE FEMORAL COMPONENT.

    Patient problems: Joint Laxity

    MAUDE report 15531670 ↗
  • InjuryJan 12, 2018Loose or Intermittent Connection

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

    Patient problems: No Code Available

    MAUDE report 7185760 ↗

Other PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER devices

All PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER devices →

Sources and updates

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