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DJO SURGICAL 344-10-710Recalls & reported problems

Encore Medical, L.P. · EMPOWR CR KNEETM TIBIAL INSERT, LEFT, SIZE 10, 10MM · 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 00190446215172), received between Sep 15, 2020 and Jan 22, 2021 — classified as 2 injuries.

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

  • Appropriate Device Problem Term/Code Not Available1
  • Insufficient Device Problem Information1

Patient problems

  • Unspecified Infection2

Recent adverse event reports

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

  • InjuryJan 22, 2021Appropriate Device Problem Term/Code Not Available

    REVISION SURGERY - DUE TO POST-OP INFECTION.

    Patient problems: Unspecified Infection

    MAUDE report 11217707 ↗
  • InjurySep 15, 2020Insufficient Device Problem Information

    REVISION SURGERY - DUE TO AN INFECTION.

    Patient problems: Unspecified Infection

    MAUDE report 10534882 ↗

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

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