Continuum® Trilogy® Allofit® Longevity® 00-8751-010-36Recalls & reported problems

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00889024149137), received between Aug 18, 2021 and Sep 3, 2025 — classified as 4 injuries, 4 malfunctions.

The most frequently reported specific device problem is “Difficult to Insert” (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 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

• InjurySep 3, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT APPROXIMATELY EIGHT YEARS POST-IMPLANTATION, THE PATIENT UNDERWENT A HIP REVISION DUE TO PAIN AND DIFFICULTIES WITH ADLS. ALL COMPONENTS WERE REVISED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: Pain

  MAUDE report 22955087 ↗
• InjuryJun 6, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT APPROXIMATELY EIGHT YEARS POST-IMPLANTATION, THE PATIENT UNDERWENT A HIP REVISION DUE TO PAIN AND DIFFICULTIES WITH ADLS. ALL COMPONENTS WERE REVISED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: Pain

  MAUDE report 22157344 ↗
• InjuryJun 20, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THE PATIENT UNDERWENT AN INITIAL HIP ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT WAS REVISED EIGHT (8) YEARS POST IMPLANTATION DUE TO PAIN. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: Pain

  MAUDE report 19578732 ↗
• MalfunctionOct 5, 2023Difficult to Insert; Difficult to Insert

  NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17878521 ↗
• InjuryJan 7, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT EXPERIENCED SEVERE PAIN FROM THE HIP, A SEVERE LIMP, AND DIFFICULTY WITH AMBULATION APPROXIMATELY 7 YEARS POST IMPLANTATION. HOWEVER, NO REVISION HAS BEEN REPORTED TO DATE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Ambulation or Postural Difficulties; Pain

  MAUDE report 13193902 ↗
• MalfunctionNov 23, 2021Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT DURING AN INITIAL HIP PROCEDURE THE LINER WOULD SEAT INTO THE SHELL. THE SURGEON REMOVED THE LINER AND REPLACED WITH A BACKUP LINER WITH NOT COMPLICATIONS. NO ADVERSE EVENTS HAVE BEEN REPORTED AS A RESULT OF THE MALFUNCTION. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION TO THE REPORTED EVEN IS UNAVAILABLE AT THIS TIME

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12860140 ↗
• MalfunctionOct 14, 2021Device Contaminated During Manufacture or Shipping; Device Contaminated During Manufacture or Shipping

  NO ADDITIONAL INFORMATION ON THE REPORTED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12632009 ↗
• MalfunctionAug 18, 2021Positioning Failure; Positioning Failure

  UPON RECEIPT OF ADDITIONAL INFORMATION, IT WAS DETERMINED THIS PRODUCT SHOULD NOT HAVE BEEN REPORTED UNDER THIS MFR NUMBER. THIS REPORT SHOULD BE VOIDED AND A CORRECTED REPORT WILL BE FILED UNDER MFR NUMBER 2648920.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12339036 ↗

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.