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DJO SURGICAL 412-02-053Recalls & reported problems

Encore Medical, L.P. · SHELL, BIPOLAR, MODULAR, ENCORE, SIZE53 · Class 2 · Implant

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

Adverse event reports
3
Deaths reported
0
Injuries reported
3
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00888912077446), received between Sep 20, 2019 and Apr 22, 2022 — classified as 3 injuries.

The most frequently reported specific device problem is “Unstable” (1 report).

18 other recalls cover devices cleared under the same FDA submission (K953510); 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

Device problems

  • Appropriate Device Problem Term/Code Not Available3
  • Unstable1

Patient problems

  • Unspecified Infection2
  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • InjuryApr 22, 2022Appropriate Device Problem Term/Code Not Available

    REVISION SURGERY - DUE TO INFECTION, REVISION OF HEMI WAS DONE. REMOVED AND EXCHANGED OUT THE BIPOLAR AND HEAD.

    Patient problems: Unspecified Infection

    MAUDE report 14188551 ↗
  • InjuryDec 13, 2019Appropriate Device Problem Term/Code Not Available

    REVISION SURGERY - PATIENT HAD INFECTION.

    Patient problems: Unspecified Infection

    MAUDE report 9466970 ↗
  • InjurySep 20, 2019Unstable; Appropriate Device Problem Term/Code Not Available

    REVISION SURGERY - DUE TO INSTABILITY. CONVERSION OF HEMIARTHROPLASTY TO TOTAL HIP ARTHROPLASTY.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9099475 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K953510. One submission often covers many models, so check the product and lot details in each record.

  • Z-0094-2008 · Aug 2, 2007 · Terminated
    Foundation Hip System Bipolar Modular, Size 52mm OD; Cat. #412-01-052; Sterile; assembly required by physician prior to implant; manufactured by Encore Medical, L.P., Austin, TX 7
  • Z-0088-2008 · Aug 2, 2007 · Terminated
    Foundation Hip System Bipolar Modular, Size 46mm OD; Cat. #412-01-046; Sterile; assembly required by physician prior to implant; manufactured by Encore Medical, L.P., Austin, TX 7
  • Z-0084-2008 · Aug 2, 2007 · Terminated
    Foundation Hip System Bipolar Modular, Size 42mm OD; Cat. #412-01-042; Sterile; assembly required by physician prior to implant; manufactured by Encore Medical, L.P., Austin, TX 7
  • Z-0083-2008 · Aug 2, 2007 · Terminated
    Foundation Hip System Bipolar Modular, Size 41mm OD; Cat. #412-01-041; Sterile; assembly required by physician prior to implant; manufactured by Encore Medical, L.P., Austin, TX 7
  • Z-0090-2008 · Aug 2, 2007 · Terminated
    Foundation Hip System Bipolar Modular, Size 48mm OD; Cat. #412-01-048; Sterile; assembly required by physician prior to implant; manufactured by Encore Medical, L.P., Austin, TX 7
  • Z-0099-2008 · Aug 2, 2007 · Terminated
    Foundation Hip System Bipolar Modular, Size 60mm OD; Cat. #412-01-060; Sterile; assembly required by physician prior to implant; manufactured by Encore Medical, L.P., Austin, TX 7
  • Z-0091-2008 · Aug 2, 2007 · Terminated
    Foundation Hip System Bipolar Modular, Size 49mm OD; Cat. #412-01-049; Sterile; assembly required by physician prior to implant; manufactured by Encore Medical, L.P., Austin, TX 7
  • Z-0093-2008 · Aug 2, 2007 · Terminated
    Foundation Hip System Bipolar Modular, Size 51mm OD; Cat. #412-01-051; Sterile; assembly required by physician prior to implant; manufactured by Encore Medical, L.P., Austin, TX 7
  • Z-0095-2008 · Aug 2, 2007 · Terminated
    Foundation Hip System Bipolar Modular, Size 53mm OD; Cat. #412-01-053; Sterile; assembly required by physician prior to implant; manufactured by Encore Medical, L.P., Austin, TX 7
  • Z-0089-2008 · Aug 2, 2007 · Terminated
    Foundation Hip System Bipolar Modular, Size 47mm OD; Cat. #412-01-047; Sterile; assembly required by physician prior to implant; manufactured by Encore Medical, L.P., Austin, TX 7
  • Z-0085-2008 · Aug 2, 2007 · Terminated
    Foundation Hip System Bipolar Modular, Size 43mm OD; Cat. #412-01-043; Sterile; assembly required by physician prior to implant; manufactured by Encore Medical, L.P., Austin, TX 7
  • Z-0087-2008 · Aug 2, 2007 · Terminated
    Foundation Hip System Bipolar Modular, Size 45mm OD; Cat. #412-01-045; Sterile; assembly required by physician prior to implant; manufactured by Encore Medical, L.P., Austin, TX 7
  • Z-0086-2008 · Aug 2, 2007 · Terminated
    Foundation Hip System Bipolar Modular, Size 44mm OD; Cat. #412-01-044; Sterile; assembly required by physician prior to implant; manufactured by Encore Medical, L.P., Austin, TX 7
  • Z-0082-2008 · Aug 2, 2007 · Terminated
    Foundation Hip System Bipolar Modular, Size 40mm OD; Cat. #412-01-040; Sterile; assembly required by physician prior to implant; manufactured by Encore Medical, L.P., Austin, TX 7
  • Z-0098-2008 · Aug 2, 2007 · Terminated
    Foundation Hip System Bipolar Modular, Size 58mm OD; Cat. #412-01-058; Sterile; assembly required by physician prior to implant; manufactured by Encore Medical, L.P., Austin, TX 7

…and 3 more.

Other Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented devices

All Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented devices →

Sources and updates

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