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DJO SURGICAL 932-34-250Recalls & reported problems

Encore Medical, L.P. · LINER, ACETABULAR, HOODED, NEUTRAL, 10°, HXL/FMP, 34MM ID, MP6 · 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 00888912100052), received between Apr 8, 2020 and Apr 8, 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

  • Appropriate Device Problem Term/Code Not Available1
  • Device Dislodged or Dislocated1

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.

  • InjuryApr 8, 2020Device Dislodged or Dislocated; Appropriate Device Problem Term/Code Not Available

    SECOND REVISION SURGERY - PATIENT HAD POSSIBLE INFECTION AND HAD DISLOCATED.

    Patient problems: Unspecified Infection

    MAUDE report 9938697 ↗

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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