Continuum® Trilogy® Allofit® Longevity® 00-8752-013-32Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889024149809), received between Mar 16, 2021 and Jul 5, 2024 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Difficult to Insert” (1 report).

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.

• MalfunctionJul 5, 2024Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT INTRAOPERATIVELY, A TITANIUM CUP (IT CUP) OF 56 WAS FIRST USED, AND THEN AN ATTEMPT WAS MADE TO IMPLANT THE CORRESPONDING POLYETHYLENE LINER, AND IT WAS FOUND THAT THE POLYETHYLENE LINER AND THE CUP OF 56 COULD NOT BE LOCKED, SO THE CUP WAS REMOVED AND AN ATTEMPT WAS MADE TO IMPLANT THE POLYETHYLENE LINER OUTSIDE OF THE BODY, AND IT WAS FOUND THAT IT COULD NOT BE LOCKED, AND THEN THE SURGEON WENT BACK TO USING THE LARGER FILE, AND IMPLANTED A CUP OF 58, AND PUNCHED THE 58 CORRESPONDING POLYETHYLENE LINER, AND IT WAS NOT ABLE TO BE LOCKED. THE DOCTOR HAD NO CHOICE BUT TO REMOVE IT, INCREASE THE SIZE OF THE FILE, AND FINALLY USED A 60 CUP AND THE CORRESPONDING LINER TO LOCK IT IN PLACE. IT WAS REPORTED TO CAUSE A SIXTY (60) MINUTE DELAY. NO OTHER HARM TO THE PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19680035 ↗
• InjuryMar 16, 2021Malposition of Device; Malposition of Device

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

  Patient problems: Pain

  MAUDE report 11496863 ↗