Navitracker Kit A : Knee
Brand(s)
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:
Alert / recall type
Health product recall
Category
Health products - Medical devices - 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
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