Continuum® Trilogy® Allofit® Longevity® 00-8752-006-28Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889024149632), received between Sep 18, 2023 and May 7, 2025 — classified as 2 injuries.

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 18, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryMay 7, 2025Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT THE LINER WOULDN'T FIT INSIDE THE CUP. IN THE PROCESS OF INSERTING, THE ACETABULAR WALL WAS FRACTURED. AS A RESULT, THE PATIENT WILL NEED TO UNDERGO ANOTHER PROCEDURE TO CORRECT THE ADVERSE EVENT. NO FURTHER INTERVENTION HAS BEEN REPORTED TO DATE. THERE IS NO FURTHER INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Bone Fracture(s)

  MAUDE report 21976120 ↗
• InjurySep 18, 2023Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THE LINER DID NOT FIX IN THE CUP AND WHILE FIXING THE LINER, THE ACETABULAR WALL OF THE PATIENT BROKE. THE SURGERY WAS DELAYED TWO (2) HOURS. SURGEON HAD TO ABANDON THE CASE AND THE PATIENT WILL NEED ANOTHER SURGERY. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: Bone Fracture(s)

  MAUDE report 17764742 ↗