G7 Acetabular Liner 010000818Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00880304526082), received between Feb 11, 2022 and Apr 2, 2025 — 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 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.

• MalfunctionApr 2, 2025Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT THE LINER WOULD NOT LOCK INTO PLACE WITH THE SHELL. THE PROCEDURE WAS COMPLETED USING A NEW LINER. DUE DILIGENCE IS IN PROGRESS FOR THIS COMPLAINT; TO DATE NO ADDITIONAL INFORMATION OR PRODUCT HAS BEEN RECEIVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21751902 ↗
• MalfunctionFeb 11, 2022Difficult to Insert; Difficult to Insert

  IT WAS REPORTED DURING A HIP PROCEDURE THE LINER FELL OUT OF THE SHELL AFTER REPEATED ATTEMPTS TO DRIVE IT IN. A NEW LINER WAS USED TO COMPLETE THE SURGERY, WITH APPROXIMATELY 30 MINUTES OF DELAY. 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 13514898 ↗