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Continuum® Trilogy® Allofit® Longevity® 00-8751-014-36Recalls & reported problems

Zimmer, Inc. · Class 2 · Implant

All models of Continuum Trilogy Allofit Longevity (39)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00889024149274), received between Apr 13, 2022 and Apr 13, 2022 — classified as 1 injury.

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

Device problems

  • Appropriate Device Problem Term/Code Not Available1

Patient problems

  • Ambulation or Postural Difficulties1
  • Pain1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryApr 13, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    IT WAS REPORTED THAT PATIENT IS SUFFERING FROM PAIN, LIMPING, AND IS NOT HAPPY WITH THE IMPLANTS AFTER AN UNKNOWN AMOUNT OF TIME POST INITIAL HIP PROCEDURE. PATIENT REPORTS HAVING SEEN MANY DIFFERENT DOCTORS AND ATTENDED MANY PHYSICAL THERAPY SESSIONS WITH NO PROGRESS. NO REVISION SURGERY HAS BEEN REPORTED TO DATE. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

    Patient problems: Ambulation or Postural Difficulties; Pain

    MAUDE report 14103946 ↗

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.

Other Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented devices

All Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page