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G7 FREEDOM ACETABULAR LINER 110010284Recalls & reported problems

Biomet Orthopedics, LLC · Class 2 · Implant

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00880304544598), received between Nov 21, 2022 and Feb 7, 2023 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Difficult to Insert” (2 reports).

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

  • Difficult to Insert2

Patient problems

  • No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionFeb 7, 2023Difficult to Insert; Difficult to Insert

    NO ADDITIONAL EVENT INFORMATION TO REPORT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16311598 ↗
  • MalfunctionNov 21, 2022Difficult to Insert; Difficult to Insert

    THERE IS NO UPDATE TO THE PREVIOUS EVENT DESCRIPTION PROVIDED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15833012 ↗

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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