JOURNEY 74023242Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 03596010555076), received between Jan 6, 2020 and Jun 19, 2024 — classified as 4 injuries.

The most frequently reported specific device problem is “Degraded” (1 report).

4 other recalls cover devices cleared under the same FDA submission (K042515, K230653); 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

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryJun 19, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT, AFTER A TKA SURGERY HAD BEEN PERFORMED ON (B)(6) 2013, THE PATIENT UNDERWENT A REVISION SURGERY ON (B)(6) 2024, DURING WHICH THE PATELLA WAS RESURFACED USING A 35 MM JOURNEY PATELLA, AND ONE (1) JOURN ART INS BCS STD 3-4 LT10 WAS EXCHANGED FOR AN 11MM INSERT. THE REASON LEADING TO THE REVISION SURGERY IS UNKNOWN. THE PATIENT'S CURRENT HEALTH STATUS IS UNKNOWN.

  Patient problems: Insufficient Information

  MAUDE report 19567299 ↗
• InjuryJul 4, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT, AFTER A TKA SURGERY HAD BEEN PERFORMED ON (B)(6) 2012, A JOURN ART INS BCS STD 3-4 LT10 WAS EXCHANGED DUE TO DISLOCATION. THE ADVERSE EVENT WAS ADDRESSED WITH A REVISION SURGERY ON (B)(6) 2022 TO REPLACE THE INSERT. THE CONDITION OF THE PATIENT IS UNKNOWN.

  Patient problems: Joint Dislocation

  MAUDE report 14907067 ↗
• InjuryMar 2, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A REVISION SURGERY WAS PERFORMED IN (B)(6) 2020 DUE TO IMPLANT FAILURE. INSERT WAS ORIGINALLY IMPLANTED IN A FEMALE PATIENT IN 2008.

  Patient problems: Injury

  MAUDE report 9774028 ↗
• InjuryJan 6, 2020Degraded; Degraded

  IT WAS REPORTED THAT PATIENT HAD A REVISION SURGERY PERFORMED DUE TO METALLOSIS AND INSERT WEAR.

  Patient problems: Injury

  MAUDE report 9551101 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K042515, K230653. One submission often covers many models, so check the product and lot details in each record.

• Z-2621-2023 · Aug 31, 2023 · Open, Classified
  smith&nephew LEGION OXINUM POSTERIOR STABILIZED NONPOROUS FERMOAL COMPONENT, SIZE 5N, LEFT, NARROW, REF 71421265; knee joint
• 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
• 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-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