G7 Acetabular Liner 010000942Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00880304527164), received between Jul 2, 2020 and Dec 8, 2025 — classified as 2 injuries, 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryDec 8, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  NO FURTHER INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Ambulation or Postural Difficulties; Pain

  MAUDE report 23737364 ↗
• MalfunctionJan 3, 2023Positioning Failure; Difficult to Insert; Positioning Failure; Difficult to Insert

  IT WAS REPORTED THAT THE LINER WOULD NOT ENGAGE IN THE CUP UPON IMPACTION. ANOTHER LINER WAS OPENED, AND THE IMPACTION WAS SUCCESSFUL. NO DEBRIS FELL NOR WAS THERE ANY CONSEQUENCES OR IMPACT TO THE PATIENT. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16088085 ↗
• InjuryJul 2, 2020Unstable; Detachment of Device or Device Component; Noise, Audible; Unstable; Detachment of Device or Device Component; Noise, Audible

  IT WAS REPORTED PATIENT UNDERWENT A HIP REVISION APPROXIMATELY FOUR MONTHS POST IMPLANTATION DUE TO POLY LINER DETACHMENT FROM CUP. DURING THE PROCEDURE, THE HEAD WAS NOTED TO HAVE ARTICULATED ON THE METAL CUP, SO BOTH THE HEAD AND LINER COMPONENTS WERE REMOVED AND REPLACED. PATIENT EXPERIENCED DISCOMFORT AND RESTRICTED DAILY ACTIVITIES. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Discomfort; Limited Mobility Of The Implanted Joint; Pain; Reaction; Swelling

  MAUDE report 10224499 ↗