JOURNEY II XR 74023860Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00885556615744), received between Apr 30, 2020 and Sep 22, 2021 — classified as 2 injuries.

1 other recall cover devices cleared under the same FDA submission (K152726, 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjurySep 22, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT, AFTER A TKA SURGERY, A PATIENT UNDERWENT A REVISION SURGERY ON (B)(6) 2017 DUE TO LEFT KNEE PAIN AND STIFFNESS. THIS ISSUE WAS RESOLVED. FURTHER INFORMATION IS NOT AVAILABLE AT THIS TIME.

  Patient problems: Loss of Range of Motion

  MAUDE report 12513246 ↗
• InjuryApr 30, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PATIENT PRESENTED LEFT KNEE PATELLAR IMPINGEMENT AND CREPITUS. EVENT WAS TREATED WITH IRRIGATION AND DEBRIDEMENT.

  Patient problems: Injury

  MAUDE report 10014582 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K152726, 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