Health product recall

Navitracker Kit A : Knee

Last updated

Summary

Product
Navitracker Kit A : Knee
Issue
Medical devices - Increased risk or new adverse events
What to do

Contact the manufacturer if you require additional information.

Affected products

Affected Products

Lot or serial number

Model or catalog number

Navitracker Kit A : Knee

110221A1

20-8000-000-07

Issue

Zimmer Biomet is conducting a medical device recall for one lot of the Navitracker Kit A : Knee product, which is a nonpatient contacting device used during computer and robotic assisted surgeries. The product in scope was released for distribution without passing sterilization results. this could potentially lead to insufficient sterility of the product, which may lead to the risks identified.

Recall start date: Jan 13, 2022

Additional information

Details
Original published date: 2022-01-25
Alert / recall type
Health product recall
Category
Health product - Medical device - Neurology
Companies

Orthosoft Ulc, Dba Zimmer Cas

75 Queen Street, Montreal, Quebec

Canada, H3C 2N6

Published by
Health Canada
Audience
General public
Health professionals
Hospitals
Recall class
Type II
Identification number
RA-63858