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U.S. Department of Health and Human Services

Class 2 Device Recall Magnifuse Bone Graft

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  Class 2 Device Recall Magnifuse Bone Graft see related information
Date Initiated by Firm July 31, 2023
Date Posted September 08, 2023
Recall Status1 Open3, Classified
Recall Number Z-2524-2023
Recall Event ID 92846
510(K)Number K082615  
Product Classification Filler, bone void, calcium compound - Product Code MQV
Product Magnifuse Bone Graft, Large, Size: 14mm x 25mm, REF 7509014, Human Tissue, Demineralized Bone Matrix, sterile.
Code Information Serial numbers: A57958-011, A57958-012, A57958-013, A57958-014, A57958-015, A57958-016, A57958-017, A57958-018, A57958-019, A57958-020, A57958-021, A57958-022, A57958-023, A57958-024, A57958-025, A57958-026, A57958-027, A57958-028, A57958-029, A57958-030, A57958-031, A57958-033, A57958-034, A57958-035, A57958-036, A57958-037, A57958-038, A57958-048, A57958-050, A57958-051, A57958-052, A57958-053, A57958-054, A57958-055, A57958-056, A57958-057, A57958-058, A57958-059, A57958-060, A57958-066, A57958-069, A57958-070, A57958-072, A57958-073, A57958-074, A57958-075, A57958-076, A57958-077, A57958-078, A57958-079, A57958-080, A57958-081, A57958-082, A57958-085, A57958- 086. Exp. 2/15/2025. UDI-DI 00613994986467
Recalling Firm/
Medtronic Sofamor Danek USA Inc
1800 Pyramid Pl
Memphis TN 38132-1703
Manufacturer Reason
for Recall
The incorrect product labeling was applied to the product indicating the wrong size of product.
FDA Determined
Cause 2
Process control
Action Beginning 7/31/2023, In the U.S. Medtronic initiated a Consignee Notification and Customer Confirmation Form via UPS 2-Day delivery to each listed consignee. Consignees were asked to quarantine and return any affected unused product they may have and complete and return the Customer Confirmation Form (i.e. reply form). Additionally, consignees were asked to forward this notification to those who need to be aware within the organization or to any location which the devices have been transferred.
Quantity in Commerce 55 pouches
Distribution US Nationwide distribution in the states of ID, IN, MN, NC, NY, OH, OR, WA, and WI.
Total Product Life Cycle TPLC Device Report

1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
510(K) Database 510(K)s with Product Code = MQV and Original Applicant = OSTEOTECH INC