JOURNEY 71932926Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00885556057971), received between Jan 30, 2020 and Feb 12, 2021 — classified as 1 injury, 1 malfunction.

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 12, 2021Break; Break

  IT WAS REPORTED THAT DURING TKA PROCEDURE THE PEG OF THE JRNY 7.5 RND RSF PAT TL 32 STD BROKE OFF WHILE USE INSIDE THE PATIENT. THERE WAS A DELAY OF LESS THAN 30 MIN. A S&N BACK UP DEVICE WAS AVAILABLE TO COMPLETE THE PROCEDURE. NO FURTHER COMPLICATIONS WERE REPORTED AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11321281 ↗
• MalfunctionJan 30, 2020Break; Break

  IT WAS REPORTED THAT DURING A TKA PROCEDURE, THE PEG BROKE OFF AS THE TRIAL WAS BEING REMOVED. ALL THE PIECES WERE RECOVERED. A BACKUP DEVICE WAS NOT REQUIRED. THERE WAS NO DELAY IN THE PROCEDURE AND NO PATIENT INJURIES WERE REPORTED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9649542 ↗