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JOURNEY 71932910Recalls & reported problems

Smith & Nephew, Inc. · JOURNEY 7.5 ROUND RESURF PAT 26MM STANDARD · 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 00885556059913), received between Jul 29, 2020 and Jul 29, 2020 — classified as 1 injury.

3 other recalls cover devices cleared under the same FDA submission (K042515); 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

  • Cellulitis1
  • Injury1
  • Swelling/ Edema1
  • Unspecified Infection1

Recent adverse event reports

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

  • InjuryJul 29, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT CELLULITIS ON THE RIGHT KNEE AND LEG HAD PRESENTED. PATIENT DEVELOPED REDNESS AND SWELLING OF THE LEG. ADMITTED TO HOSPITAL FOR ANTIBIOTICS. EVENTUALLY RESOLVED WITHOUT LONG TERM PROBLEMS. HOME PHYSICAL THERAPY AND MEDICATION WERE PRESCRIBED FOR TREATMENT.

    Patient problems: Cellulitis; Injury; Swelling/ Edema; Unspecified Infection

    MAUDE report 10339811 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K042515. One submission often covers many models, so check the product and lot details in each record.

  • Z-0002-2019 · Jun 13, 2018 · Open, Classified
    JOURNEY BCS OXINIUM Knee Femoral Components, Catalog Numbers: 74021110, 74021111, 74021112, 74021113, 74021114, 74021115, 74021116, 74021117, 74021118, 74021119, 74021120, 7402112
  • Z-0001-2019 · Jun 13, 2018 · Open, Classified
    Journey BCS Knee CoCr Femoral Components, Catalog Numbers: 74021210, 74021211, 74021212, 74021213, 74021214, 74021215, 74021216, 74021217, 74021218, 74021219, 74021220, 74021221, 7
  • Z-0003-2019 · Jun 13, 2018 · Open, Classified
    JOURNEY BCS Knee Conventional Polyethylene Inserts: 74023111, 74023112, 74023113, 74023114, 74023115, 74023116, 74023117, 74023118, 74023121, 74023122, 74023123, 74023124, 7402312

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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