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G7 OSSEOTI ACETABULAR SHELL 110010241Recalls & reported problems

Biomet Orthopedics, LLC · Class 2 · Implant

Data updated Oct 13, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00880304544161), received between Aug 28, 2023 and Aug 28, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fracture” (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

  • Fracture1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionAug 28, 2023Fracture; Fracture

    THERE IS NO UPDATE TO THE PRIOR EVENT DESCRIPTION PROVIDED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17631882 ↗

Other Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented devices

All Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented devices →

Sources and updates

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