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JOURNEY 71934523Recalls & reported problems

Smith & Nephew, Inc. · REVISION JOURNEY ARTICULAR INSERT BCS STD 3-4 LT 18MM · 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 00885556182017), received between Feb 18, 2019 and Feb 18, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).

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

  • Insufficient Device Problem Information1

Patient problems

  • Pain1
  • Swelling1

Recent adverse event reports

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

  • InjuryFeb 18, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

    IT WAS REPORTED THAT PATIENT WAS HAVING KNEE PAIN, REDNESS AND SWELLING, AND AN INCISION AND DRAINAGE OF THE LEFT KNEE WITH ARTHROCENTESIS WAS PERFORMED DUE TO PROXIMAL LEG ABCESS WITH SECONDARY CELLULITIS ADJACENT TO TOTAL KNEE ARTHROPLASTY.

    Patient problems: Pain; Swelling

    MAUDE report 8348730 ↗

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

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

Sources and updates

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