Skip to content

DJO SURGICAL 233-08-105Recalls & reported problems

Djo, LLC · 3D KNEE CEMENTED FEMORAL COMPONENT, TiNbN COATED, SZ 5, LEFT · Class 2 · Implant

All models of DJO SURGICAL (42)

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 00888912111324), received between Mar 27, 2020 and Mar 27, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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

  • Device Dislodged or Dislocated1

Patient problems

  • No Code Available1

Recent adverse event reports

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

  • InjuryMar 27, 2020Device Dislodged or Dislocated

    REVISION SURGERY - PATIENT KEPT DISLOCATING MEDIO LATERAL. TOOK OUT 3D FEMUR AND INSERT, AND REPLACED WITH A P.S FEMUR AND INSERT.

    Patient problems: No Code Available

    MAUDE report 9889257 ↗

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