G7 Acetabular Liner 010000926Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00880304527027), received between Dec 6, 2023 and Sep 11, 2026 — classified as 2 injuries, 4 malfunctions.

The most frequently reported specific device problem is “Difficult to Insert” (3 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 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• InjurySep 11, 2026Device Dislodged or Dislocated

  It was reported the patient underwent a hip revision approximately 6 years and 7 months post-implantation due to recurrent dislocation. The acetabular liner and femoral head were exchanged to a dual mobility construct. Attempts have been made and no further information has been provided.

  Patient problems: Joint Dislocation

  MAUDE report 50725446 ↗
• InjurySep 4, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A RIGHT TOTAL HIP ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT WAS REVISED THREE (3) YEARS POST IMPLANTATION DUE TO DISLOCATION. THE PATIENT HAS A STIFF SPINE CAUSING DISLOCATIONS.

  Patient problems: Joint Dislocation

  MAUDE report 20140660 ↗
• MalfunctionJul 25, 2024Difficult to Insert; Difficult to Insert

  NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19828447 ↗
• MalfunctionJul 9, 2024Packaging Problem; Packaging Problem

  IT WAS REPORTED THAT THERE WAS A HAIR FOUND ON THE FOAM RUBBER COVER INSIDE THE STERILE PACKAGING. THE DEVICE WAS IMPLANTED SINCE ITS PRIMARY PACKAGING WAS NOT COMPROMISED.THERE IS NO ADDITIONAL INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19701218 ↗
• MalfunctionMar 5, 2024Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT DURING SURGERY, THE LINER WOULD NOT ANCHOR TO THE CUP. A DIFFERENT LINER WAS USED TO COMPLETE THE PROCEDURE. THERE WAS NO KNOWN IMPACT OR CONSEQUENCES TO THE PATIENT. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18837735 ↗
• MalfunctionDec 6, 2023Difficult to Insert; Difficult to Insert

  NO FURTHER INFORMATION AT THE TIME OF THIS REPORT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18276776 ↗