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Avenir Complete™ 574203050Recalls & reported problems

Zimmer, Inc. · Class 2 · Implant

All models of Avenir Complete (37)

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 00889024509306), received between Aug 16, 2023 and Aug 16, 2023 — 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 18, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Bone Fracture(s)1

Recent adverse event reports

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

  • InjuryAug 16, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THE PATIENT UNDERWENT A HIP PROCEDURE. SUBSEQUENTLY, THE PATIENT WAS REVISED ONE MONTH POST IMPLANTATION DUE TO POST OP FEMORAL PERIPROSTHETIC FRACTURE FOUND AROUND THE FEMORAL STEM. OPTED FOR FEMORAL REVISION FOR ORIF OF FEMORAL FRACTURE AND FIXATION WITH LONG FEMORAL REVISION HIP STEMS.

    Patient problems: Bone Fracture(s)

    MAUDE report 17558920 ↗

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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