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G7 Acetabular Liner 010000744Recalls & 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 00880304525016), received between Nov 9, 2021 and Nov 9, 2021 — 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.

  • MalfunctionNov 9, 2021Difficult to Insert; Difficult to Insert

    IT WAS REPORTED THAT THE SURGEON IMPLANTED A 66MM G7 OSSEOTI MULTIHOLE CUP. SURGEON CHOSE A 40MM G7 NEUTRAL LINER. THE LINER WOULD NOT LOCK DOWN COMPLETELY. ONLY HAD 1 ON SHELF SO SURGEON REMOVED LINER WITH A 6.5MM SCREW AND REPLACED IT WITH A 36MM G7 NEUTRAL LINER WITH THE SAME RESULT. 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 12779465 ↗

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.