G7® Acetabular System 110017108Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00880304672154), received between May 3, 2021 and Sep 21, 2022 — classified as 2 malfunctions.

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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 21, 2022Difficult to Insert; Difficult to Insert

  NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15461161 ↗
• MalfunctionMay 3, 2021Material Deformation; Material Deformation

  IT WAS REPORTED THAT DURING A SURGERY WHEN PREPARING THE CUP FOR INSERTION, DURING THE REMOVAL OF THE SCREW HOLE COVERS, TWO OF THEM WERE STUCK AND SUBSEQUENTLY STRIPPED IN THE CUP. THE CUP WAS REMOVED AND A NEW ONE WAS INSERTED WITHOUT INCIDENT. 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 11766142 ↗