G7® Longevity® 20123605Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00889024519329), received between Aug 22, 2023 and Oct 17, 2025 — classified as 2 injuries, 5 malfunctions.

The most frequently reported specific device problem is “Difficult to Insert” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• InjuryOct 17, 2025Adverse 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: Hematoma

  MAUDE report 23323630 ↗
• MalfunctionJul 7, 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 22411382 ↗
• MalfunctionFeb 26, 2025Difficult to Insert; Difficult to Insert

  NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21470651 ↗
• InjuryJan 27, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED A PATIENT HAD AN INITIAL LEFT TOTAL HIP ARTHROPLASTY. SUBSEQUENTLY, WHILE GETTING UP FROM A CHAIR, FELT A SUDDEN ONSET OF PAIN AND INABILITY TO BEAR WEIGHT. THE EMERGENCY DEPARTMENT CONFIRMED THE DISLOCATION AND WAS UNABLE TO REDUCE THE HIP. THE PATIENT UNDERWENT A SUCCESSFUL REDUCTION UNDER GENERAL ANESTHESIA AND ALL IMPLANTS REMAIN IN PLACE.

  Patient problems: Ambulation or Postural Difficulties; Joint Dislocation; Pain

  MAUDE report 21242463 ↗
• MalfunctionJan 13, 2025Packaging Problem; Packaging Problem

  IT WAS REPORTED THAT THE HI WALL LINER HAD FOREIGN MATERIAL ON IT UPON OPENING THE PACKAGING. THE FOREIGN MATERIAL WAS A GREY FLAKE. THERE WAS NO REPORTED PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21139750 ↗
• MalfunctionJan 11, 2024Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT DURING RIGHT HIP SURGERY, THE LINER WOULD NOT ENGAGE WITH THE CUP. THE LINER WENT IN AND WAS FLUSH BUT WOULD POP OUT AS SOON AS THE HIP WAS RELOCATED AND PUT THROUGH A RANGE OF MOTION. THREE ATTEMPTS WERE MADE WITH THE SAME RESULT. THE LINER WAS REPLACED WITH A NEW ONE AND WORKED PROPERLY. IT WAS ALSO REPORTED THAT SURGICAL TECHNIQUE WAS UTILIZED. THERE WAS NO PATIENT IMPACT, NO SURGICAL DELAY, AND NO SURGICAL COMPLICATIONS. THE PATIENT'S ANATOMY DID NOT CONTRIBUTE TO THE EVENT. NO ADDITIONAL INFORMATION AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18491104 ↗
• MalfunctionAug 22, 2023Packaging Problem; Packaging Problem

  NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17595378 ↗