G7® Acetabular System 110010265Recalls & reported problems

Summary

The FDA's MAUDE database contains 10 adverse event reports that list this exact device (DI 00887868356032), received between May 31, 2022 and Feb 10, 2026 — classified as 9 injuries, 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 10 most recent of 10 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 10, 2026Device Dislodged or Dislocated

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

  Patient problems: Hematoma; Joint Dislocation; Medical device site infection; Periprosthetic fracture

  MAUDE report 24303607 ↗
• InjuryAug 12, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT THE CUP AND LINER WERE SEPARATED IN THE BODY. A REVISION SURGERY WAS PERFORMED TO REPLACE THE IMPLANTS. THE LINER AND HEAD WERE REPLACED IN THIS REVISION SURGERY. THE G7 CUP CONTINUES TO BE USED.

  Patient problems: Failure of Implant

  MAUDE report 22783297 ↗
• InjuryApr 7, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THERE IS NO UPDATE TO THE PRIOR EVENT DESCRIPTION PROVIDED.

  Patient problems: Bone Fracture(s)

  MAUDE report 21784332 ↗
• InjuryFeb 25, 2025Fracture; Adverse Event Without Identified Device or Use Problem; Fracture; Adverse Event Without Identified Device or Use Problem

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

  Patient problems: Bone Fracture(s); Failure of Implant

  MAUDE report 21462841 ↗
• InjuryFeb 18, 2025Adverse Event Without Identified Device or Use Problem; Loosening of Implant Not Related to Bone-Ingrowth; Adverse Event Without Identified Device or Use Problem; Loosening of Implant Not Related to Bone-Ingrowth

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION PROCEDURE 1 YEAR AND 8 MONTHS POST IMPLANTATION DUE TO INSTABILITY THAT WAS CAUSED BY THE ACETABULAR DEFECT FROM THE PREVIOUS BONE FRACTURE WHICH THEN CONTRIBUTED TO THE LOOSENING OF THE CUP. THERE IS NO ADDITIONAL INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Failure of Implant; Osteolysis

  MAUDE report 21392212 ↗
• InjuryDec 3, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A PATIENT RECEIVED A CORTISONE INJECTION TO HIS LEFT HIP APPROXIMATELY THIRTEEN MONTHS POST IMPLANTATION DUE TO TROCHANTERIC BURSITIS.

  Patient problems: Bursitis; Pain; Unequal Limb Length

  MAUDE report 20833327 ↗
• InjuryOct 31, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THERE IS NO UPDATE TO THE PRIOR EVENT DESCRIPTION PROVIDED.

  Patient problems: Bone Fracture(s); Fall

  MAUDE report 20578057 ↗
• InjuryNov 7, 2023Off-Label Use; Malposition of Device; Off-Label Use; Malposition of Device

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

  Patient problems: Failure of Implant; Joint Dislocation

  MAUDE report 18082897 ↗
• InjuryMay 16, 2023Detachment of Device or Device Component; Detachment of Device or Device Component

  NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16939953 ↗
• MalfunctionMay 31, 2022Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT DURING A HIP PROCEDURE, THE LINER WOULD NOT SEAT IN THE CUP. THE SURGEON HIT THE IMPLANTS SO HARD THAT IT DISLODGED THE CUP. A NEW LARGER CUP AND LINER WERE USED TO COMPLETE THE SURGERY. 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 14548606 ↗