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OXINIUM 71341939Recalls & reported problems

Smith & Nephew, Inc. · OXINIUM FEMORAL HEAD 10/12 32MM -5 EXTENSION · Class 2 · Implant

All models of OXINIUM (36)

Data updated Oct 16, 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 00885556112458), received between Jul 11, 2020 and Jul 11, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Mechanical Problem” (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 16, 2026.

Most reported problems

Device problems

  • Mechanical Problem1

Patient problems

  • Injury1
  • Pain1

Recent adverse event reports

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

  • InjuryJul 11, 2020Mechanical Problem; Mechanical Problem

    IT WAS REPORTED THAT A REVISION SURGERY HAD TO BE PERFORMED DUE TO PAIN, SWELLING AND DISLOCATION. THIS CASE IS NOT CAUSED BY S+N DEVICES DEFECT. SURGEON DOES NOT FAULT THE DEVICES.

    Patient problems: Injury; Pain

    MAUDE report 10261754 ↗

Other Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented devices

All Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented devices →

Sources and updates

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