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Continuum® Trilogy® Allofit® Vivacit-E® 00-8852-012-36Recalls & reported problems

Zimmer, Inc. · Class 2 · Implant

All models of Continuum Trilogy Allofit Vivacit-E (18)

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 00889024155589), received between Apr 15, 2022 and Apr 15, 2022 — classified as 1 injury.

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.

  • InjuryApr 15, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE PATIENT WAS REVISED DUE TO PAIN AND POOR CUP POSITION APPROXIMATELY 2 YEARS POST IMPLANTATION. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.

    Patient problems: Pain

    MAUDE report 14117314 ↗

Other Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented devices

All Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented devices →

Sources and updates

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