G7 Acetabular Liner 110017185Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00880304673199), received between Mar 18, 2024 and Mar 18, 2024 — 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.

• MalfunctionMar 18, 2024Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT DURING SURGERY, THE SURGEON IMPLANTED A NEUTRAL LINER BUT WANTED TO SWITCH TO AN OFFSET LINER. THE SURGEON ATTEMPTED TO IMPLANT TWO OFFSET LINERS, AND NEITHER WOULD LOCK IN. A NEUTRAL LINER WAS IMPLANTED AND THERE WAS ABOUT A 30 MINUTE DELAY. 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 18923903 ↗
• MalfunctionMar 18, 2024Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT DURING SURGERY, THE SURGEON IMPLANTED A NEUTRAL LINER BUT WANTED TO SWITCH TO AN OFFSET LINER. THE SURGEON ATTEMPTED TO IMPLANT TWO OFFSET LINERS, AND NEITHER WOULD LOCK IN. A NEUTRAL LINER WAS IMPLANTED AND THERE WAS ABOUT A 30 MINUTE DELAY. 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 18923900 ↗