G7® Longevity® 20124006Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00889024519381), received between May 21, 2021 and Aug 14, 2025 — classified as 1 injury, 3 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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 14, 2025Device Contaminated During Manufacture or Shipping; Device Contaminated During Manufacture or Shipping

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

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22809632 ↗
• MalfunctionOct 1, 2024Difficult to Insert; Material Integrity Problem; Difficult to Insert; Material Integrity Problem

  IT WAS REPORTED THAT DURING SURGERY, THE LINER WOULD NOT LOCK INTO THE CUP. THE DOCTOR SAID HE SAW IRREGULARITIES ON THE LINER LIKE THE PLASTIC WAS NOT FORMED CORRECTLY. A SECOND LINER WAS ABLE TO BE IMPLANTED. 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 20344448 ↗
• MalfunctionMay 18, 2022Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT DURING A LEFT HIP PROCEDURE, THE LINER WOULD NOT SEAT IN THE CUP. THE SURGEON HIT SO HARD DURING ATTEMPTS TO SEAT THE LINER THAT THE CUP DISLODGED. THE SURGEON HAD TO IMPLANT A LARGER CUP AND LINER AS A RESULT. THERE WAS NO REPORTED HARM OR INJURY TO THE PATIENT. 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 14427980 ↗
• InjuryMay 21, 2021Material Erosion; Unstable; Noise, Audible; Patient Device Interaction Problem; Material Erosion; Unstable; Noise, Audible; Patient Device Interaction Problem

  T WAS REPORTED THE PATIENT STATED SHE UNDERWENT A THA. SUBSEQUENTLY, PATIENT UNDERWENT A REVISION 3 MONTHS LATER. SURGEON REPORTED THAT LINER HAD DISSOCIATED AND THERE WAS DIRECT CERAMIC HEAD CONTACT WITH SHELL, LEADING TO METALLOSIS, METALLIC DEBRIS, IMPLANT WEAR TO SHELL, AND PSEUDOTUMOR. NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Ambulation or Postural Difficulties; Failure of Implant; Metal Related Pathology; Pain; Subluxation

  MAUDE report 11862342 ↗