Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Magnifuse Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to The incorrect product labeling was applied to the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Medtronic Sofamor Danek USA Inc directly.
Affected Products
Magnifuse Bone Graft, Large, Size: 14mm x 25mm, REF 7509014, Human Tissue, Demineralized Bone Matrix, sterile.
Quantity: 55 pouches
Why Was This Recalled?
The incorrect product labeling was applied to the product indicating the wrong size of product.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medtronic Sofamor Danek USA Inc
Medtronic Sofamor Danek USA Inc has 81 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report