Continuum® Trilogy® Allofit® Longevity® 00-8751-012-36Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889024149199), received between Nov 25, 2020 and May 16, 2022 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Naturally Worn” (1 report).

3 other recalls cover devices cleared under the same FDA submission (K091508, K123019, K151448); they may or may not involve this specific model.

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 16, 2022Naturally Worn; Naturally Worn

  IT WAS REPORTED THAT PATIENT DEVELOPED ELEVATED METAL IONS AND UNDERWENT A LEFT HIP REVISION APPROXIMATELY 3 YEARS POST IMPLANTATION. DURING THE PROCEDURE, ALTR, TRUNNION CORROSION AND LINER WEAR WERE FOUND. THE STEM AND CUP REMAINED WELL FIXED. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Failure of Implant; Osteolysis

  MAUDE report 14410017 ↗
• MalfunctionNov 25, 2020Positioning Failure; Positioning Failure

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

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 10904845 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K091508, K123019, K151448. One submission often covers many models, so check the product and lot details in each record.

• Z-0094-2015 · Oct 1, 2014 · Terminated
  Continuum Acetabular System Trabecular Metal Shell with Multi Holes, Porous 68mm, Prosthesis, Hip, Semi-Constrained, Metal/Polymer
• Z-0071-2011 · Mar 19, 2010 · Terminated
  Continuum Acetabular Systems Shell Inserter Adapter with Rotational Control, 00-8790-003-00, Zimmer Inc., Warsaw, IN. Used to mate the inserter with the shell implant.
• Z-0072-2011 · Mar 19, 2010 · Terminated
  Continuum Acetabular Systems Shell Inserter Adapter without Rotational Control, 00-8790-003-10, Zimmer Inc., Warsaw, IN. Used to mate the inserter with the shell implant.