G7® Dual Mobility Acetabular System 110024462Recalls & reported problems

Summary

The FDA's MAUDE database contains 22 adverse event reports that list this exact device (DI 00880304703506), received between Jul 8, 2021 and Aug 26, 2026 — classified as 18 injuries, 4 malfunctions.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (10 reports).

1 FDA recall record name this device's identifier, 1 still open.

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 18, 2026.

Recalls naming this device

1. Feb 6, 2023Class IIOpen, Classified

   The outer package labeling and product etch are a 40 mm Size D liner, however, the implant is a 38 mm Size C liner.

   Z-1284-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 22 most recent of 22 reports, in the reporter's own words as published by the FDA.

• InjuryAug 26, 2026Device Dislodged or Dislocated

  It was reported that the patient underwent a hip revision approximately 1-year post-implantation due to joint dislocation. Initially, the surgeon attempted to reduce the dislocation; however, an intraprosthetic dislocation occurred. Subsequently, the liner and DM bearing were revised. No additional information available for the reported event.

  Patient problems: Joint Dislocation

  MAUDE report 50460045 ↗
• MalfunctionJan 22, 2026Packaging Problem

  IT WAS REPORTED THAT WHEN REMOVING THE PRODUCT, THE STERILIZATION TRAY CONTAINING THE PRODUCT WAS DEFORMED, CAUSING THE OUTER AND INNER CASES TO BECOME STUCK TOGETHER. THIS RESULTED IN A 3 MINUTE DELAY; PRODUCT WAS USED, AND PACKAGE WAS DISCARDED. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24156562 ↗
• InjuryJan 12, 2026Device Dislodged or Dislocated

  IT WAS REPORTED THAT APPROXIMATELY SIX WEEKS POST-IMPLANTATION, THE PATIENT UNDERWENT A CLOSED REDUCTION DUE HIP DISLOCATION. THE PATIENT SUFFERED TWO PREVIOUS DISLOCATIONS AND THE LATEST OCCURRED WHEN THEY WERE LYING IN BED AND TURNED ONTO THEIR HIP. THE HIP WAS REDUCED UNDER GENERAL ANESTHESIA WITHOUT DIFFICULTY. FOLLOWING THE PROCEDURE, WHEN PERFORMING TRACTIONS, THERE WAS SOME SUBLUXATION SO THE HIP WAS IMMOBILIZED TO NOT FLEX THE HIP. THE FOLLOWING DAY, IT WAS RE-EVALUATED AND THE THIGH WAS LIFTED WITHOUT PROBLEM OR PAIN. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: Joint Dislocation

  MAUDE report 24032907 ↗
• InjuryOct 24, 2025Material Erosion; Device Dislodged or Dislocated; Material Erosion; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT UNDERWENT HIP REVISION APPROXIMATELY 2 YEARS POST IMPLANTATION DUE TO DISLOCATION. UPON OPENING THE JOINT CAPSULE, A METALLOSIS REACTION WAS OBSERVED. PART OF THE DM (DUAL MOBILITY) POLY BEARING HAD FRACTURED, FORMING A HELMET-LIKE SHAPE, AND THE CERAMIC HEAD HAD BECOME DETACHED. ADDITIONALLY, A PARTIALLY WORN SCRATCH WAS NOTED ON THE STEM NECK. NO ADDITIONAL INFORMATION AVAILABLE FOR THE REPORTED EVENT.

  Patient problems: Joint Dislocation; Metal Related Pathology

  MAUDE report 23377928 ↗
• InjurySep 2, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL HIP PROCEDURE ON AN UNKNOWN DATE. SUBSEQUENTLY, THE PATIENT WAS REVISED DUE TO PAIN. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: Pain

  MAUDE report 22937321 ↗
• InjuryJul 10, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT APPROXIMATELY FOUR YEARS POST-IMPLANTATION, THE PATIENT UNDERWENT A HIP REVISION DUE TO DISLOCATION OF THE LINER AND BEARING. THE SURGEON ATTEMPTED A MANUAL REDUCTION OF THE DISLOCATION AND THEN THE BEARING AND HEAD SEPARATED. ALL COMPONENTS REVISED EXCEPT THE STEM. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: Joint Dislocation

  MAUDE report 22472961 ↗
• InjuryJun 18, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A PATIENT HAD AN INITIAL LEFT TOTAL HIP ARTHROPLASTY. AT 2 YEARS POSTOP, THE PATIENT REPORTS ONGOING MODERATE LOW BACK PAIN THAT WAS NOT PRESENT PRIOR TO THE INITIAL PROCEDURE. IT WAS INITIALLY THOUGHT TO BE GENERAL POSTOP SORENESS, BUT THE PAIN HAS NOT RESOLVED AND CONTINUES TO LIMIT DAILY ACTIVITIES. THE PATIENT HAS STARTED THERAPY FOR THE LOW BACK PAIN, TAKES NSAIDS FOR PAIN, AND USES A CANE FOR LONG DISTANCES. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: Pain

  MAUDE report 22284959 ↗
• InjuryJun 9, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THE PATIENT UNDERWENT A HIP ARTHROPLASTY AND WAS IMPLANTED WITH ZIMMER BIOMET PRODUCTS. SUBSEQUENTLY, THE PATIENT WAS REVISED NEARLY ONE (1) YEAR POST IMPLANTATION DUE TO DISLOCATION. THE LINER WAS EXPLANTED.

  Patient problems: Joint Dislocation

  MAUDE report 22168787 ↗
• InjuryFeb 7, 2025Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION PROCEDURE DUE TO UNKNOWN REASONS. THERE IS NO ADDITIONAL INFORMATION AVAILABLE AT THIS TIME.

  Patient problems: Insufficient Information

  MAUDE report 21332495 ↗
• InjuryOct 24, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THE PATIENT UNDERWENT A HIP ARTHROPLASTY AND WAS IMPLANTED WITH ZIMMER BIOMET PRODUCTS. SUBSEQUENTLY, THE PATIENT WAS REVISED DUE TO DISLOCATION FIVE (5) YEARS POST IMPLANTATION. THE CAUSE FOR THE DISLOCATION IS UNKNOWN. THE STEM, HEAD, AND BEARINGS WERE REPLACED. THERE WERE NO CONTRIBUTING CONDITIONS RELATED TO THE EVENT.

  Patient problems: Joint Dislocation

  MAUDE report 20521418 ↗
• InjuryOct 15, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL HIP ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT WAS REVISED DUE TO THE DISASSOCIATION OF THE DUAL MOBILITY LINER ONE (1) YEAR POST IMPLANTATION DUE TO A FALL.

  Patient problems: Joint Dislocation

  MAUDE report 20452727 ↗
• InjurySep 11, 2024Device Dislodged or Dislocated; Naturally Worn; Device Dislodged or Dislocated; Naturally Worn

  IT WAS REPORTED THAT APPROXIMATELY ONE YEAR AND FIVE MONTHS POST RIGHT TOTAL HIP ARTHROSCOPY, THE PATIENT DEVELOPED PAIN AND HAD A DISASSOCIATION. THERE WAS NO ADDITIONAL INFORMATION AVAILABLE RELATED TO THE INITIAL DISASSOCIATION. SUBSEQUENTLY, APPROXIMATELY ONE MONTH AGO, THE PATIENT PRESENTED TO THE EMERGENCY DEPARTMENT WITH A DISLOCATION. THE HEAD WAS RELOCATED; HOWEVER, THE X-RAY SHOWED A DISASSOCIATION. THE PATIENT WAS REVISED AND DURING THE PROCEDURE, A LARGE AMOUNT OF METALLOSIS WITH SOME DAMAGE TO THE NECK OF THE STEM WAS NOTED. THE HEAD WAS OBSERVED TO HAVE SIGNIFICANT METAL DEBRIS AND HAD DISASSOCIATED FROM THE BEARING. THE BEARING SHOWED DAMAGE AND WAS FLOATING IN SOFT TISSUE. WEAR WAS ALSO NOTED TO THE LINER, WHICH MADE IT DIFFICULT TO REMOVE. THE STEM NECK WAS FOUND TO BE IMPINGING ON THE LINER RIM. FURTHER DAMAGE WAS CAUSED DURING REMOVAL, AS THE SUCTION CUP AND VIBRATION TECHNIQUES FAILED. AN OSTEOTOME WAS USED TO REMOVE THE DAMAGED LINER. THE SURGEON DECIDED THAT FURTHER CONSTRAINT WAS REQUIRED DUE TO THE SOFT TISSUE DAMAGE CAUSED BY THE METALLOSIS. EXTENSIVE DEBRIDEMENT WAS MADE, AND THE HEAD AND LINER WERE INSERTED, AND THE STEM WAS REVISED. NO ADDITIONAL INFORMA

  Patient problems: Failure of Implant; Joint Dislocation; Metal Related Pathology; Pain; Unspecified Tissue Injury

  MAUDE report 20190620 ↗
• InjurySep 9, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

  Patient problems: Pain

  MAUDE report 20168961 ↗
• MalfunctionJan 4, 2024Separation Failure; Separation Failure

  IT WAS REPORTED THAT THE DUAL MOBILITY RING FOR THE LINER WAS STUCK IN THE SHELL. IT HAD TO BE REMOVED WITH OTHER INSTRUMENTS. THE PROCEDURE WAS COMPLETED WITH A DIFFERENT SHELL AND LINER. 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 18443661 ↗
• InjuryMar 24, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT DISLOCATED WHILE BEING MOVED AFTER THE PRIMARY SURGERY. THE BEARING, LINER, STEM AND HEAD WERE REMOVED AND REPLACED WITHOUT FURTHER COMPLICATIONS. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: Joint Dislocation

  MAUDE report 16609244 ↗
• MalfunctionOct 17, 2022Difficult to Insert; Difficult to Insert

  NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15615663 ↗
• InjuryOct 11, 2022Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION PROCEDURE SAME DAY AS THE INITIAL IMPLANTATION DUE TO THE LINER BECOMING DISLODGED. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Failure of Implant

  MAUDE report 15576831 ↗
• InjuryApr 4, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT PATIENT UNDERWENT A LEFT HIP REVISION APPROXIMATELY 7 MONTH POST IMPLANTATION DUE TO DISLOCATION. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Joint Dislocation

  MAUDE report 13993498 ↗
• InjuryOct 12, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

  Patient problems: Seroma

  MAUDE report 12614767 ↗
• InjurySep 22, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  NO ADDITIONAL INFORMATION ON THE REPORTED EVENT.

  Patient problems: Unspecified Infection

  MAUDE report 12513004 ↗
• InjurySep 22, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  NO ADDITIONAL INFORMATION ON THE REPORTED EVENT.

  Patient problems: Unspecified Infection

  MAUDE report 12512950 ↗
• MalfunctionJul 8, 2021Difficult to Insert; Difficult to Insert

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

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12134347 ↗