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Continuum® Trilogy® Allofit® Longevity® 00-8751-012-40Recalls & 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 00889024149205), received between Oct 12, 2021 and Oct 12, 2021 — 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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Pain1

Recent adverse event reports

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

  • InjuryOct 12, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE PATIENT EXPERIENCED SEVERE PAIN AND WAS DIAGNOSED WITH TROCHANTERIC BURSITIS APPROXIMATELY SIX (6) MONTHS POST IMPLANTATION. THE SURGEON RECOMMENDED PHYSICAL THERAPY, REST, AND ICE. THE OUTCOME WAS TOLERATED, AND THE PATIENT SHOWED IMPROVEMENT AT THE ONE (1) YEAR FOLLOW UP WITH MODERATE PAIN. ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.

    Patient problems: Pain

    MAUDE report 12614949 ↗

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/POLYMER, POROUS UNCEMENTED devices

All PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED devices →

Sources and updates

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