Navitracker Kit A : Knee recall in Canada: Increased risk of adverse events
In plain language
This recall involves the Navitracker Kit A : Knee, a medical device used in surgeries. It's being recalled because it was released without passing sterilization results, which could lead to insufficient sterility. Stop using the product and contact the manufacturer for more information.
What to do
- Stop using the product immediately.
- Contact the manufacturer for additional information.
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Affected products
Navitracker Kit A : Knee
Model: 20-8000-000-07
Lot: 110221A1
Why this matters
Increased risk or new adverse events
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the lot number
Lot numbers identify specific production batches.
Affected lots: 110221A1
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 20-8000-000-07
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
Increased risk or new adverse events
What should consumers do?
Stop using the product immediately. Contact the manufacturer for additional information.
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
Yes, there may be a health risk. Increased risk or new adverse events
When was this product recalled?
This product was recalled on January 24, 2022.
Is the Orthosoft ULC, Dba Zimmer Cas brand affected by this recall?
Yes, Orthosoft ULC, Dba Zimmer Cas products are affected by this recall. This recall involves the Navitracker Kit A : Knee, a medical device used in surgeries. It's being recalled because it was released without passing sterilization results, which could lead to insufficient sterility. Stop using the product and contact the manufacturer for more information.