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JOURNEY 71934526Recalls & reported problems

Smith & Nephew, Inc. · REVISION JOURNEY ARTICULAR INSERT BCS STD 5-6 RT 11MM · Class 2 · Implant

All models of JOURNEY (566)

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 00885556182161), received between Oct 15, 2020 and Oct 15, 2020 — 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

  • Unspecified Infection1

Recent adverse event reports

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

  • InjuryOct 15, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT A REVISION SURGERY IS NEEDED FOR A PATIENT DUE TO INFECTION. POLY EXCHANGE IS REQUIRED. THIS WAS NOTICED DURING A INSPECTION IN THE TKA PROCEDURE SO THE CASE IS CURRENTLY DELAYED SINCE PATIENT HAVE NOT RECEIVED THE REPLACEMENT. THERE IS NO MORE INFORMATION PROVIDED FOR THIS EVENT AT THIS TIME.

    Patient problems: Unspecified Infection

    MAUDE report 10681892 ↗

Other PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER devices

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Sources and updates

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