Grafton and Grafton Plus Demineralized Bone Matrix
In plain language
This recall involves Grafton and Grafton Plus Demineralized Bone Matrix sold in Canada. It's being recalled because of a potential breach in the sterile barrier. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Contact the manufacturer if you require additional information.
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Affected products
Specific affected products are listed in the official notice.
Why this matters
Performance issue
Do I have this product?
This recall applies to specific products. Details are listed in the official notice.
Frequently Asked Questions
Why was this product recalled?
Performance issue
What should consumers do?
Stop using the product immediately. 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 Grafton and Grafton Plus Demineralized Bone Matrix sold in Canada. It's being recalled because of a potential breach in the sterile barrier. Stop using the product and follow the return/repair steps in the official notice.