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Reliance 6265-3-112Recalls & reported problems

Howmedica Osteonics Corp. · Cemented Hip Stem · Class 2 · Implant

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 04546540262868), received between Sep 9, 2019 and Sep 9, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Loosening of Implant Not Related to Bone-Ingrowth” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Loosening of Implant Not Related to Bone-Ingrowth1

Patient problems

  • Injury1

Recent adverse event reports

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

  • InjurySep 9, 2019Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth

    IT WAS REPORTED THAT THE PATIENT'S RIGHT HIP WAS REVISED DUE TO LOOSENING OF THE FEMORAL STEM. INTRA-OPERATIVELY, THE STEM WAS EASILY REMOVED FROM THE PATIENT. THE STEM (ORIGINALLY CEMENTED WITH SIMPLEX P CEMENT), CERAMIC HEAD, AND CERAMIC. LINER WERE REVISED TO AN ADM/ MDM LINER CONSTRUCT AND COMPETITOR STEM AND HEAD. REP CONFIRMED THERE ARE NO ALLEGATIONS AGAINST THE REVISED HEAD AND LINER.

    Patient problems: Injury

    MAUDE report 8975907 ↗

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

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

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.