Oxford Partial Knee System recall in Canada: Sterility issue
In plain language
This recall involves the Oxford Partial Knee System, Fixed Lateral Tibial Construct sold in Canada. It's being recalled because of a potential sterility issue due to incorrect packaging. This product is for healthcare use only.
What to do
- Contact the manufacturer, Biomet UK Limited, for additional information.
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Affected products
Oxford Partial Knee System, Fixed Lateral Tibial Construct
Model: 154341
Lot: 077830
Why this matters
Sterility issue
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: 077830
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 154341
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?
Sterility issue
What should consumers do?
Contact the manufacturer, Biomet UK Limited, 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. Sterility issue
When was this product recalled?
This product was recalled on January 2, 2023.
Is the Biomet Uk Limited brand affected by this recall?
Yes, Biomet Uk Limited products are affected by this recall. This recall involves the Oxford Partial Knee System, Fixed Lateral Tibial Construct sold in Canada. It's being recalled because of a potential sterility issue due to incorrect packaging. This product is for healthcare use only.