JOURNEY 71934537Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885556182710), received between Dec 17, 2020 and Dec 17, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (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

Recent adverse event reports

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

• InjuryDec 17, 2020Break; Break

  IT WAS REPORTED THAT THE PATIENT PRESENTED ON (B)(6) 2020 WITH A DISLOCATED TKR AFTER CROSSING LEGS IN A FIGURE 4 POSITION. SURGEON TRIED A CLOSED REDUCTION WITH NO SUCCESS SO PATIENT WAS BOOKED FOR OPEN REDUCTION THE NEXT DAY. THE OLD POLY WAS REMOVED AND IT WAS NOTICED THAT IT WAS BROKEN. A NEW JOURNEY REVISION INSERT WAS IMPLANTED. NO OTHER COMPLICATIONS WERE REPORTED. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED ACCORDINGLY.

  Patient problems: Failure of Implant; Joint Dislocation

  MAUDE report 11027275 ↗