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PERSONA® Vivacit-E® 42-5121-004-12 (UDI 00889024235588)Recalls & reported problems

Zimmer, Inc. · Class 2 · Implant

All models of PERSONA Vivacit-E (285)

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 00889024235588), received between Apr 17, 2019 and Apr 17, 2019 — 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

  • Abdominal Pain1
  • Cardiac Arrest1
  • Death1
  • Nausea1
  • Pulmonary Embolism1
  • Thrombosis1
  • Thrombosis/Thrombus1
  • Vomiting1

Recent adverse event reports

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

  • InjuryApr 17, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

    Patient problems: Abdominal Pain; Cardiac Arrest; Death; Nausea; Pulmonary Embolism; Thrombosis; Thrombosis/Thrombus; Vomiting

    MAUDE report 8523540 ↗

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Sources and updates

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