G7 Acetabular Liner 110017220Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00880304673519), received between Sep 7, 2021 and Sep 7, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 18, 2026.

Most reported problems

Recent adverse event reports

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

• InjurySep 7, 2021Device Dislodged or Dislocated; Naturally Worn; Device Dislodged or Dislocated; Naturally Worn

  IT WAS REPORTED THAT PATIENT UNDERWENT A RIGHT HIP REVISION DUE TO PAIN AND METAL RELATED PATHOLOGY APPROXIMATELY 7 YEARS POST IMPLANTATION. SUBSEQUENTLY, THE PATIENT VISITED THE EMERGENCY ROOM DUE TO DISLOCATIONS, PAIN AND SWELLING WITH NO NOTED MEDICAL INTERVENTION. THE PATIENT THEN UNDERWENT A SECOND REVISION APPROXIMATELY 4 YEARS LATER DUE TO CHRONIC INFECTION. ALL DEVICES WERE REMOVED AND REPLACED WITH SPACERS. APPROXIMATELY 1 MONTH LATER THE PATIENT STILL HAD ONGOING INFECTION DESPITE USE OF ANTIBIOTICS, SO NEW SPACERS WERE IMPLANTED ALONG WITH WIRES. THERE IS NO REPORT OR NEW PERMANENT IMPLANTS BEING IMPLANTED TO DATE. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Joint Dislocation; Scar Tissue; Sepsis

  MAUDE report 12432254 ↗