Infinity Occipitocervical Upper Thoracic System Multi Axial Screw
In plain language
This recall involves the Infinity Occipitocervical Upper Thoracic System Multi Axial Screw sold in Canada. It's being recalled because an incorrect material was used, which may reduce its strength and lead to a loss of fixation. This recall is for healthcare professionals.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Infinity Occipitocervical Upper Thoracic System Multi Axial Screw
Model: 3604024
Lot: H5802983
Why this matters
Performance 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: H5802983
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 3604024
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?
Performance issue
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. Performance issue
When was this product recalled?
This product was recalled on March 1, 2023.
Is the Medtronic Sofamor Danek Usa, Inc. brand affected by this recall?
Yes, Medtronic Sofamor Danek Usa, Inc. products are affected by this recall. This recall involves the Infinity Occipitocervical Upper Thoracic System Multi Axial Screw sold in Canada. It's being recalled because an incorrect material was used, which may reduce its strength and lead to a loss of fixation. This recall is for healthcare professionals.