G7® Longevity® 20103606Recalls & reported problems

Summary

The FDA's MAUDE database contains 15 adverse event reports that list this exact device (DI 00889024518759), received between Mar 27, 2020 and Oct 6, 2025 — classified as 8 injuries, 7 malfunctions.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (3 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 15 most recent of 15 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 6, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated

  NO ADDITIONAL INFORMATION AVAILABLE FOR THE REPORTED EVENT.

  Patient problems: Joint Dislocation

  MAUDE report 23223161 ↗
• MalfunctionSep 8, 2025Manufacturing, Packaging or Shipping Problem; Manufacturing, Packaging or Shipping Problem

  NO FURTHER INFORMATION AT THE TIME OF THIS REPORT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22991167 ↗
• InjuryJan 14, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  ADDITIONAL INFORMATION RECEIVED. IT WAS REPORTED THAT THE PATIENT¿S OSSIFICATION SITE WAS SEEN ON PRE-OPERATIVE IMAGES AND THE PATIENT HAS BEEN THROUGH THE COURSE OF RADIOGRAPHIC IMAGING, INCLUDING A RECENT CT SCAN COMPLETED APPROXIMATELY TWO MONTHS AGO. IT WAS REPORTED THAT THERE WAS NO TRAUMA OR OTHER SPECIFIC CONTRIBUTING FACTORS WHICH COULD EXPLAIN THE SYMPTOMS. PATIENT WAS DESCRIBED AS A HEALTHY, FULLY COMPLIANT PERSON WITH GOOD MOTIVATION AND FOCUS ON POSTOP REHABILITATION. THE PATIENT HAS A NORMAL ACTIVITY LEVEL AND REGULAR CONTACT WITH PHYSIO. THE PATIENT IS NOW SCHEDULED TO HAVE AN ULTRASOUND GUIDED INJECTION AT THE OSSIFICATION SITE FOR DIAGNOSTIC PURPOSES. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: Extraskeletal ossification; Pain

  MAUDE report 21154899 ↗
• InjuryMay 1, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED A PATIENT RECEIVED A CORTISONE INJECTION APPROXIMATELY THREE MONTHS POST IMPLANTATION FOR LATERAL HIP PAIN AND TROCHANTERIC BURSITIS. THEN AGAIN ONE YEAR POST IMPLANTATION DUE TO MILD PAIN, MODERATE DIFFICULTIES WITH ADL¿S, SNAPPING SENSATION AND DIFFICULTY SLEEPING. THE PATIENT WAS PRESCRIBED A CORTICOSTEROID INJECTION IN THE RIGHT TROCHANTERIC BURSA, VOLTAREN GEL AND A PRESCRIPTION FOR PT, POSSIBLY DRY NEEDLING. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: Bursitis; Pain; Swelling/ Edema

  MAUDE report 19222871 ↗
• MalfunctionApr 10, 2024Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT DURING THE PROCEDURE, THE LINER WOULD NOT ASSEMBLE WITH THE SHELL AFTER SEVERAL ATTEMPTS. THE PROCEDURE WAS COMPLETED WITH ANOTHER LINER. THERE WAS NO HARM OR HEALTH CONSEQUENCES TO THE PATIENT. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19077913 ↗
• 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 19010930 ↗
• InjuryMar 11, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

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

  Patient problems: Bursitis; Pain

  MAUDE report 18876626 ↗
• InjuryJan 31, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT APPROXIMATELY TWO WEEKS POST IMPLANTATION OF A RIGHT TOTAL HIP ARTHROPLASTY, THE PATIENT HAD A DISLOCATION. THE PATIENT WAS TREATED WITH A CLOSED REDUCTION. THE SURGEON CLASSIFIED THE EVENT AS AN ADVERSE EVENT WITH MODERATE SEVERITY AND DEFINITELY RELATED TO THE PROCEDURE. THE OUTCOME RESOLVED. APPROXIMATELY FIVE DAYS AFTER THE CLOSED REDUCTION, THE PATIENT HAD A SECOND DISLOCATION AND WAS TREATED WITH A CLOSED REDUCTION. THE SURGEON AGAIN CLASSIFIED THE EVENT AS AN ADVERSE EVENT, WITH MODERATE SEVERITY AND WAS DEFINITELY RELATED TO THE PROCEDURE. THE OUTCOME WAS RESOLVED. NO ADDITIONAL INFORMATION WAS AVAILABLE.

  Patient problems: Joint Dislocation; Nerve Damage; Pain

  MAUDE report 18616766 ↗
• MalfunctionSep 5, 2023Difficult to Insert; Difficult to Insert

  NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17685707 ↗
• MalfunctionApr 25, 2023Device Contaminated During Manufacture or Shipping; Device Contaminated During Manufacture or Shipping

  NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16805929 ↗
• InjuryMay 24, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT PATIENT WAS BENDING AND TWISTING WHEN THEY FELT A POP AND INCREASED PAIN IN LEFT HIP APPROXIMATELY 6 WEEKS POST HIP ARTHROPLASTY. THE PATIENT PRESENTED TO THE CLINIC AND WAS DIAGNOSED WITH DISLOCATION. THE PATIENT UNDERWENT A REDUCTION UNDER ANESTHESIA THE NEXT DAY. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Joint Dislocation; Pain

  MAUDE report 14487885 ↗
• InjuryFeb 25, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PATIENT DEVELOPED A PULMONARY EMBOLISM APPROXIMATELY 2 YEARS POST LEFT TOTAL HIP ARTHROPLASTY. THE PATIENT WAS HOSPITALIZED OVERNIGHT, TREATED MEDICALLY AND COMPLICATIONS RESOLVED. COMPONENTS REMAINED IMPLANTED ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Pulmonary Embolism

  MAUDE report 13597821 ↗
• MalfunctionApr 14, 2021Positioning Failure; Positioning Failure

  IT WAS REPORTED DURING AN INITIAL HIP ARTHROPLASTY THE LINER DID NOT SEAT FULLY IN CUP. SURGERY WAS COMPLETED WITH A BACKUP LINER. THE EXCHANGE WAS DONE WITHOUT ISSUE. 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 11663578 ↗
• InjuryApr 1, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT EXPERIENCED INCREASED LEFT ANTERIOR THIGH PAIN IN MODERATE INTENSITY APPROXIMATELY 6 MONTHS POST IMPLANTATION. ADDITIONAL PHYSICAL THERAPY WAS PRESCRIBED FOR SIX WEEKS FOR RECURRENT ILIOPSOAS TENDINITIS. NO REVISION PROCEDURE HAS BEEN REPORTED TO DATE. ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.

  Patient problems: Pain

  MAUDE report 11606036 ↗
• MalfunctionMar 27, 2020Positioning Failure; Positioning Failure

  NO ADDITIONAL INFORMATION ON REPORTED EVENT.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9888578 ↗