Continuum® Trilogy® Allofit® Longevity® 00-8751-009-32Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00889024149106), received between Feb 24, 2020 and Dec 13, 2023 — classified as 4 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (2 reports).

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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryDec 13, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A TOTAL HIP REPLACEMENT. SUBSEQUENTLY, THE PATIENT HAD A FALL, LANDING ON THE HIP THAT WAS REPLACED, CAUSING THE DISLOCATION. THE PATIENT UNDERWENT A REVISION PROCEDURE APPROXIMATELY 1 MONTH POST IMPLANTATION. PERIOPERATIVELY, THE SURGEON DECIDED TO EXCHANGE THE SHELL DUE TO SHELL MALPOSITION AND THE LINER FOR AN ELEVATED LINER. ON REMOVAL OF THE FEMORAL HEAD, THE STEM WAS REMOVED AND EXCHANGED FOR THE SAME OFFSET AND SIZE. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: Joint Dislocation

  MAUDE report 18317686 ↗
• InjuryOct 21, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED WAS REPORTED PATIENT RETURNED TO HOSPITAL 3 YEARS POST IMPLANTATION DUE TO RIGHT THIGH PAIN THAT RADIATES TO HIP. THE SURGEON IS UNCERTAIN IF THE EVENT IS RELATED TO THE DEVICE. TREATED INITIALLY WITH CONSERVATIVE MONITORING, BUT SINCE PAIN IS PERSISTENT, IMAGING AND BONE SCAN TAKEN WITH RESULTS PENDING AT TIME OF REPORTING. PATIENT REPORTS CONTINUED SEVERE PAIN. ALL WORKUP FOR INFECTION HAVE BEEN NEGATIVE AND REASONS FOR THE PAIN THUS FAR INCONCLUSIVE. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Pain

  MAUDE report 12671454 ↗
• InjuryJun 23, 2020Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THE LINER WOULD NOT SEAT INTO THE CUP. NO ADVERSE EVENTS HAVE BEEN REPORTED AS A RESULT OF THE MALFUNCTION. ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 10184163 ↗
• InjuryFeb 24, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION PROCEDURE APPROXIMATELY 2 YEARS AND 2 MONTHS POST IMPLANTATION DUE TO DISLOCATION. NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Joint Dislocation

  MAUDE report 9744721 ↗

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-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.
• 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.