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DJO SURGICAL 933-36-256Recalls & reported problems

Encore Medical, L.P. · LINER, ACETABULAR, 20 DH, HXL/FMP, 36MM ID 56MM CUP OD, MP9 · 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 00888912100632), received between Oct 11, 2017 and Oct 11, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Metal Shedding Debris” (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

  • Metal Shedding Debris1

Patient problems

  • No Code Available1
  • Pain1

Recent adverse event reports

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

  • InjuryOct 11, 2017Metal Shedding Debris

    REVISION SURGERY - DUE TO THE PATIENT HAVING SIGNIFICANT METALLOSIS AND PAIN.

    Patient problems: No Code Available; Pain

    MAUDE report 6941438 ↗

Other Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented devices

All Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented devices →

Sources and updates

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