Skip to content

OXINIUM 71341941Recalls & 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 00885556112434), received between Nov 1, 2021 and Nov 1, 2021 — classified as 1 injury.

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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Joint Dislocation1

Recent adverse event reports

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

  • InjuryNov 1, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT, AFTER A THR SURGERY, A REVISION SURGERY WAS PERFORMED DUE TO DISLOCATION. AN OXINIUM HD 10/12 32MM +5 EXT WAS EXPLANTED. SURGEON SAYS THAT THE DEVICES WERE NOT DEFECTIVE. CURRENT PATIENT HEALTH STATUS REMAINS UNKNOWN.

    Patient problems: Joint Dislocation

    MAUDE report 12734115 ↗

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

How reports and recalls are matched · Editorial policy · Report an error on this page