G7® Acetabular System 110010268Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00887868356063), received between Oct 3, 2023 and Jul 8, 2025 — classified as 4 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

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

  IT WAS FURTHER REPORTED THE PATIENT WAS EXPERIENCING WORSENING LEFT HIP, GROIN, BUTTOCK AND THIGH PAIN, LIMITED DAILY ACTIVITIES, AND MILD LIMP STARTING APPROXIMATELY 2 MONTHS POST-IMPLANTATION. THE PATIENT WAS ALSO NOTED TO HAVE SOME EDEMA TO THE FOOT. THE SURGEON PROVIDED A SHOE LIFT TO THE PATIENT FOR LEG LENGTH DISCREPANCY AND PATIENT CONTINUED PHYSICAL THERAPY; HOWEVER, THIS DID NOT PROVIDE ANY RELIEF. THE SURGEON REFERRED THE PATIENT TO AN ORTHOTIST FOR A CUSTOM SHOE. PATIENT ALSO PROVIDED FLECTOR PATCH FOR PAIN.

  Patient problems: Pain; Unequal Limb Length

  MAUDE report 22435140 ↗
• InjurySep 10, 2024Migration; Migration

  IT WAS REPORTED THAT APPROXIMATELY 5 MONTHS POST IMPLANTATION OF A LEFT TOTAL HIP ARTHROPLASTY, THE PATIENT IS BEING CONSIDERED FOR A REVISION DUE TO HIP PAIN AND CUP MIGRATION MEDIALLY INTO THE PELVIS. THERE ARE NO KNOWN CONTRIBUTING CONDITIONS EXCEPT FOR POOR BONE QUALITY. NO ADDITIONAL INFORMATION WAS AVAILABLE.

  Patient problems: Failure of Implant; Pain

  MAUDE report 20186166 ↗
• InjuryAug 26, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A HIP ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT SUFFERED A FALL AND WAS REVISED FOUR (4) MONTHS POST IMPLANTATION DUE TO A BONE FRACTURE. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: Bone Fracture(s)

  MAUDE report 20067296 ↗
• InjuryOct 3, 2023Naturally Worn; Insufficient Device Problem Information; Loosening of Implant Not Related to Bone-Ingrowth; Naturally Worn; Insufficient Device Problem Information; Loosening of Implant Not Related to Bone-Ingrowth

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A LEFT HIP ARTHROPLASTY ON AN UNKNOWN DATE. SUBSEQUENTLY, THE PATIENT IS BEING CONSIDERED FOR A PMI PRODUCT FOR AN UNKNOWN REASON. ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION HAVE BEEN MADE; HOWEVER, NO MORE IS AVAILABLE AT THIS TIME.

  Patient problems: Failure of Implant; Fall; Insufficient Information

  MAUDE report 17861926 ↗