JOURNEY 74033642Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00885556421918), received between Jan 14, 2020 and Jul 1, 2024 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Break” (2 reports).

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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 1, 2024Break; Break

  IT WAS REPORTED THAT, DURING TKA SURGERY, ONE (1) JRNY II CR ISRT TRL LT SZ 3-4 10M BROKE. THE PROCEDURE WAS RESUMED, WITHOUT ANY DELAY, USING A S+N BACK-UP DEVICE. NO INJURY WAS REPORTED AS A CONSEQUENCE OF THIS ISSUE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19643959 ↗
• MalfunctionDec 1, 2023Fracture; Fracture

  IT WAS REPORTED THAT ONE (1) JRNY II CR ISRT TRL LT SZ 3-4 10M IS BROKEN IN TWO PIECES. IT WAS USING A BONE TAMP TO PUT TRIAL POLY IN AND BROKE THE TRIAL POLY IN HALF. THE SURGERY WAS COMPLETED WITH A POSTED POLY, USING A CONSTRAINED TRIAL, WITHOUT ANY DELAY. NO INJURY TO PATIENT WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18247717 ↗
• MalfunctionJan 14, 2020Break; Break

  IT WAS REPORTED THAT DURING SURGERY THE TRIAL BROKE. ANY PIECE WAS LEFT INSIDE THE PATIENT. NO PATIENT INJURY OR OTHER COMPLICATIONS WERE REPORTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9588768 ↗