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DJO SURGICAL 233-02-108Recalls & reported problems

Encore Medical, L.P. · FEMUR, NONPOROUS, 3D, SIZE8, RT · 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 00888912111256), received between Nov 19, 2016 and Nov 19, 2016 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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

  • Insufficient Device Problem Information1

Patient problems

  • Unspecified Infection1

Recent adverse event reports

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

  • InjuryNov 19, 2016Insufficient Device Problem Information

    REVISION SURGERY - THE PATIENT HAD GONE TO THE DENTIST TO HAVE 2 INFECTED TEETH REMOVED AND DID NOT GET PUT ON ANY ANTIBIOTICS. THIS ENSURED AN INFECTION IN THE RIGHT KNEE, THEREFORE ALL COMPONENTS WERE REMOVED EXCEPT FOR THE PATELLA.

    Patient problems: Unspecified Infection

    MAUDE report 6115670 ↗

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

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