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G7 Acetabular Liner 010000801Recalls & reported problems

Biomet Orthopedics, LLC · Class 2 · Implant

All models of G7 Acetabular Liner (85)

Data updated Oct 16, 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 00880304525931), received between Apr 19, 2021 and Apr 19, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Positioning Failure” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Positioning Failure1

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.

  • MalfunctionApr 19, 2021Positioning Failure; Positioning Failure

    IT WAS REPORTED THAT DURING AN INITIAL PROCEDURE, THE SURGEON WAS UNABLE TO INSERT THE POLYETHYLENE LINER INTO THE ACETABULAR CUP. THE SURGEON THEN TRIED A BACKUP LINER AND IT WAS ALSO UNSUCCESSFUL. THE G7 ACETABULAR CUP WAS REPLACED WITH A MALLORY HEAD ACETABULAR CUP. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11684461 ↗

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

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Sources and updates

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