G7 Freedom Acetabular Liner 110010285Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00880304544604), received between Sep 21, 2022 and Sep 21, 2022 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Difficult to Insert” (2 reports).

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 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

  IT WAS REPORTED THE FREEDOM LINERS WOULD NOT SEAT AND LOCK REQUIRING SURGEON TO REMOVE CUP AND REPLACE WITH LARGER CUP AND DIFFERENT LINER. NO ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15461169 ↗
• MalfunctionSep 21, 2022Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THE FREEDOM LINERS WOULD NOT SEAT AND LOCK REQUIRING SURGEON TO REMOVE CUP AND REPLACE WITH LARGER CUP AND DIFFERENT LINER. NO ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15461160 ↗