G7® Acetabular System 110010246Recalls & reported problems

Summary

The FDA's MAUDE database contains 11 adverse event reports that list this exact device (DI 00887868355905), received between Nov 21, 2022 and Aug 28, 2026 — classified as 6 injuries, 5 malfunctions.

The most frequently reported specific device problem is “Patient Device Interaction Problem” (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 11 most recent of 11 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 28, 2026Product Quality Problem; Packaging Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50500322 ↗
• MalfunctionOct 29, 2025Unsealed Device Packaging; Unsealed Device Packaging

  IT WAS REPORTED THAT THE INNER PACKAGING APPEARED TO BE DISTORTED WITH A PROTRUDING SEAL. IT LOOKED LIKE AIR GOT INTO THE BOX AND IT WAS COMPROMISED. 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 23413559 ↗
• InjuryAug 5, 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: Medical device site infection; Necrosis; Pain; Scar Tissue

  MAUDE report 22722663 ↗
• MalfunctionJul 10, 2025Fracture; Fracture

  IT WAS REPORTED THAT DURING A HIP SURGERY, THE CUP FRACTURED DURING INSERTION. 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 22470589 ↗
• InjuryJun 11, 2025Patient Device Interaction Problem; Patient Device Interaction Problem

  IT WAS REPORTED THAT APPROXIMATELY TWO YEARS POST-IMPLANTATION, THE PATIENT UNDERWENT A HIP REVISION DUE TO SEVERE PAIN AND FAILED IMPLANTS. PATIENT EXPERIENCED PAIN, WEAKNESS, TROCHANTERIC BURSITIS, AND POSSIBLE ILIOPSOAS TENDINITIS. THE SHELL WAS RETAINED AND ALL OTHER IMPLANTS REVISED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: Bursitis; Failure of Implant; Inflammation; Muscle Weakness/Atrophy; Pain

  MAUDE report 22186677 ↗
• MalfunctionMay 20, 2025Separation Failure; Separation Failure

  IT WAS REPORTED THAT ONE OF THE SCREW CAPS WOULD NOT BACK OUT OF THE CUP. IT SPUN LOOSELY IN THE CUP AND THE THREADS WOULD NOT ENGAGE TO BACK THE CUP OUT. THE SURGEON OPTED TO USE A DIFFERENT CUP TO COMPLETE THE PROCEDURE. THERE IS NO FURTHER INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22051995 ↗
• InjuryMar 21, 2025Difficult to Insert; Difficult to Insert

  NO FURTHER INFORMATION AT THE TIME OF THIS REPORT.

  Patient problems: Bone Fracture(s)

  MAUDE report 21662325 ↗
• InjuryMay 23, 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: Discomfort; Pain; Unequal Limb Length

  MAUDE report 19380306 ↗
• InjuryApr 1, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT ONE YEAR POST IMPLANTATION OF A RIGHT TOTAL HIP ARTHROPLASTY, THE PATIENT REPORTED SEVERE HIP PAIN IN THE CONTRALATERAL HIP DURING A SCHEDULED FOLLOW UP FOR A CLINICAL STUDY. NO ADDITIONAL INFORMATION WAS AVAILABLE.

  Patient problems: Pain

  MAUDE report 19010908 ↗
• MalfunctionFeb 23, 2024Separation Failure; Separation Failure

  THERE IS NO UPDATE TO THE PRIOR EVENT DESCRIPTION PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18767419 ↗
• InjuryNov 21, 2022Material Erosion; Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem; Material Erosion; Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem

  IT WAS REPORTED THAT A PATIENT UNDERWENT A HIP REVISION APPROXIMATELY TWO YEARS POST IMPLANTATION DUE TO METALOSIS. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: Metal Related Pathology

  MAUDE report 15836912 ↗