Charlotte Foot And Ankle System recall in Canada: Manufacturing defect
In plain language
This recall involves Charlotte Foot And Ankle System - MTP HEX Screws, Non-Sterile, sold in Canada. It's being recalled because of a manufacturing defect where the package contains the incorrect product. Contact the manufacturer if you require additional information.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Charlotte Foot And Ankle System - MTP HEX Screws, Non-Sterile
Model: 41122718
Lot: 02010697711582591
Why this matters
Manufacturing defect
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: 02010697711582591
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 41122718
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?
Manufacturing defect
What should consumers do?
Contact the manufacturer if you require 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. Manufacturing defect
When was this product recalled?
This product was recalled on December 8, 2021.
Is the Wright Medical Technology Inc. brand affected by this recall?
Yes, Wright Medical Technology Inc. products are affected by this recall. This recall involves Charlotte Foot And Ankle System - MTP HEX Screws, Non-Sterile, sold in Canada. It's being recalled because of a manufacturing defect where the package contains the incorrect product. Contact the manufacturer if you require additional information.