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G7® Longevity® 20113204Recalls & reported problems

Zimmer, Inc. · Class 2 · Implant

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00889024518971), received between Feb 2, 2022 and Feb 2, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Off-Label Use” (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

  • Off-Label Use1
  • Unintended Movement1

Patient problems

  • Pain1

Recent adverse event reports

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

  • InjuryFeb 2, 2022Off-Label Use; Unintended Movement; Off-Label Use; Unintended Movement

    IT WAS REPORTED THE PATIENT UNDERWENT INITIAL HIP ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT WAS REVISED DUE TO PAIN, ACETABULAR COMPONENT LOOSENING, AND SOFT TISSUE IMPINGEMENT CAUSED BY INCOMPATIBLE HEAD AND LINER COMPONENT IMPLANTATION. THE CUP. LINER AND HEAD WERE REMOVED AND REPLACED. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

    Patient problems: Pain

    MAUDE report 13423901 ↗

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.