JOURNEY 74021162Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00885556531945), received between Mar 30, 2020 and Apr 8, 2024 — classified as 2 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (1 report).

1 other recall cover devices cleared under the same FDA submission (K121443, 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.

• InjuryApr 8, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT, AFTER A PATIENT WAS IMPLANTED A JRNY II CR FEM OX NP LT SZ 2 IN THE LEFT KNEE ON (B)(6) 2022, DISLOCATION OF THE KNEE OCCURRED WITHIN 10 DAYS POST OPERATIVE WHEN IN BED AND SLEEPING ON HER SIDE. CLOSED REDUCTION WAS PERFORMED AND ABOVE KNEE CAST FOR 6 WEEKS WAS APPLIED. PATIENT RECOVERED WELL AND NO FURTHER DISLOCATION OCCURRED.

  Patient problems: Joint Dislocation

  MAUDE report 19060705 ↗
• InjuryMar 30, 2020Physical Resistance/Sticking; Physical Resistance/Sticking

  IT WAS REPORTED THAT THE PATIENT WAS DIAGNOSED WITH LEFT KNEE STIFFNESS. THE SUBJECT WAS HOSPITALIZED AND MANIPULATION UNDER ANESTHESIA WAS PERFORMED TO RESOLVE THE ISSUE WITH RESIDUAL EFFECTS.

  Patient problems: Injury

  MAUDE report 9901058 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K121443, 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