Continuum® Trilogy® Allofit® Longevity® 00-8752-010-32Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00889024149717), received between May 5, 2022 and Mar 14, 2025 — classified as 2 injuries, 5 malfunctions.

The most frequently reported specific device problem is “Difficult to Insert” (4 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 18, 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.

• MalfunctionMar 14, 2025Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT DURING THE SURGERY THE LINER AND CUP WOULD NOT MATE. THE SURGEON MADE SEVERAL ATTEMPTS BY HITTING IT, RESULTING IN THE LOOSENING OF THE CUP. A NEW CUP AND LINER WERE USED, AND THE SURGERY WAS COMPLETED SUCCESSFULLY. 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 21604564 ↗
• InjuryMay 21, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION PROCEDURE 7 MONTHS AND 7 DAYS POST IMPLANTATION DUE TO MALALIGNMENT, SOCKET DISLOCATION AND SUBLUXATION. THE CUP, HEAD AND LINER WERE ALL REVISED. THERE IS NO ADDITIONAL INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Joint Dislocation

  MAUDE report 19358925 ↗
• MalfunctionApr 23, 2024Difficult to Insert; Difficult to Insert

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

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19165833 ↗
• InjuryJul 18, 2023Unstable; Unstable

  NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

  Patient problems: Failure of Implant; Unspecified Infection

  MAUDE report 17342371 ↗
• MalfunctionMay 19, 2023Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT THE LINER WOULD NOT ASSEMBLE WITH THE CUP DURING SURGERY. THERE WAS NO HARM OR DELAY REPORTED AND THE PROCEDURE WAS COMPLETED USING ANOTHER LINER AND THE SAME CUP. THERE IS NO ADDITIONAL INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16960839 ↗
• MalfunctionJul 11, 2022Difficult to Insert; Difficult to Insert

  IT WAS REPORTED AFTER STRIKING THE LINER AGAINST THE GROOVE OF THE CUP, IT WAS FOUND THAT IT COULD NOT BE ASSEMBLED IN PLACE. THE LINER WAS STRUCK AGAIN AND STILL COULD NOT BE ASSEMBLED IN PLACE. AFTER TWO REPEATED BLOWS, THE POLYETHYLENE LINED PROSTHESIS WAS ABANDONED AND ASSEMBLED FOR THE FIRST TIME AFTER SWITCHING TO A CERAMIC LINER. NO ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14978135 ↗
• MalfunctionMay 5, 2022Positioning Failure; Positioning Failure

  IT WAS REPORTED THAT AN ACETABULUM 52 WAS OPENED, AND AT THE TIME OF PLACING LINER 36, IT DID NOT FIX INSIDE THE ACETABULUM, SO A NEW LINER 32 WAS OPENED BECAUSE THE MEDICAL TEAM THOUGHT THAT LINER 36 WAS DEFECTIVE. WHEN THEY USED THE LINER 32, IT DIDN'T FIX IT IN THE ACETABULUM EITHER. THE DOCTOR TOOK OUT THE 52 ACETABULUM AND TESTED BOTH LINERS OUTSIDE THE PATIENT, AND NEITHER ONE OF THEM FIXED INSIDE THE ACETABULUM. THEY HAD TO OPEN THE 54 ACETABULUM AND THE 36 LINER TO FINISH THE SURGERY. NO ADVERSE EVENTS HAVE BEEN REPORTED AS A RESULT OF THE MALFUNCTION. 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 14287560 ↗