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G7 OSSEOTI ACETABULAR SHELL 110010267Recalls & reported problems

Biomet Orthopedics, LLC · Class 2 · Implant

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 00880304544420), received between Jul 22, 2022 and Jul 22, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Insert” (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

  • Difficult to Insert1

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.

  • MalfunctionJul 22, 2022Difficult to Insert; Difficult to Insert

    IT WAS REPORTED THAT DURING AN INITIAL HIP ARTHROPLASTY, THE LINER ALIGNMENT RING BECAME LODGED IN BETWEEN THE SHELL AND THE LINER AFTER IMPACTION. THE LINER AND BROKEN RING WERE REMOVED AND A NEW LINER WAS IMPLANTED WITHOUT ANY FURTHER COMPLICATIONS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15083411 ↗

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

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

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