PlainRecalls
FDA Devices Moderate Class II Ongoing

Magnifuse Bone Graft, Large, Size: 14mm x 25mm, REF 7509014, Human Tissue, Demineralized Bone Matrix, sterile.

Reported: September 20, 2023 Initiated: July 31, 2023 #Z-2524-2023

Product Description

Magnifuse Bone Graft, Large, Size: 14mm x 25mm, REF 7509014, Human Tissue, Demineralized Bone Matrix, sterile.

Reason for Recall

The incorrect product labeling was applied to the product indicating the wrong size of product.

Details

Units Affected
55 pouches
Distribution
US Nationwide distribution in the states of ID, IN, MN, NC, NY, OH, OR, WA, and WI.
Location
Memphis, TN

Frequently Asked Questions

What product was recalled?
Magnifuse Bone Graft, Large, Size: 14mm x 25mm, REF 7509014, Human Tissue, Demineralized Bone Matrix, sterile.. Recalled by Medtronic Sofamor Danek USA Inc. Units affected: 55 pouches.
Why was this product recalled?
The incorrect product labeling was applied to the product indicating the wrong size of product.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 20, 2023. Severity: Moderate. Recall number: Z-2524-2023.