JOURNEY 71932925Recalls & reported problems

Smith & Nephew, Inc. · JOURNEY 7.5 ROUND RESURF PAT TRL 29MM STANDARD · Class 1

All models of JOURNEY (566)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports: 2
Deaths reported: 0
Injuries reported: 0
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00885556059524), received between Apr 5, 2020 and Feb 11, 2021 — classified as 2 malfunctions.

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

Device problems

Break1
Crack1

Patient problems

Insufficient Information1
No Consequences Or Impact To Patient1

Recent adverse event reports

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

MalfunctionFeb 11, 2021Crack
IT WAS REPORTED THAT DURING SET UP/ INSPECTION IN TKA PROCEDURE THE JRNY 7.5 RND RSF PAT TL 29 STD WAS FOUND TO BE CRACKED. NO DELAY. THERE WAS A S&N BACK UP DEVICE AVAILABLE TO COMPLETE THE PROCEDURE. NO INJURIES REPORTED AT THIS TIME.
Patient problems: Insufficient Information
MAUDE report 11319808 ↗
MalfunctionApr 5, 2020Break; Break
IT WAS REPORTED THAT DURING A TKA PROCEDURE, THE 7.5 JII PATELLA TRIAL 29MM PEG BROKE WHILE IT WAS BEING USED. NO INJURIES OR SURGICAL DELAYS WERE REPORTED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9926378 ↗

Device details

UDI-DI	`00885556059524`
Brand	JOURNEY
Model	71932925
Company	Smith & Nephew, Inc.
Product code	LXH · ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	No
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Sep 7, 2023

Device type (GMDN): General internal orthopaedic fixation system implantation kit

A collection of instruments and devices intended to be used for the placement of an internal orthopaedic fixation system into or onto all types of bones (e.g., bones of limbs, spine, pelvis, or craniomaxillofacial). It is a non-dedicated device that includes various metallic and/or plastic reusable devices [e.g., retractors, rods, clamps, drills, pins, saws, screwdrivers, guides, trials, impactors] intended to be used for the implantation of any type of internal orthopaedic fixation system; the implant(s) is not included. This is a reusable device.

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All ORTHOPEDIC MANUAL SURGICAL INSTRUMENT devices →

Sources and updates

Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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