Magnifuse Bone Graft — Class II medical device recall Z-2524-2023
Ongoing recall by Medtronic Sofamor Danek USA Inc, reported 2023-09-20, distributed nationwide. The incorrect product labeling was applied to the product indicating the wrong size of product.
| Recall number | Z-2524-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Sofamor Danek USA Inc, Memphis, TN, United States |
| Recall initiated | 2023-07-31 |
| Classified | 2023-09-08 |
| Reported by FDA | 2023-09-20 |
| Distributed | Nationwide (US) |
| Quantity | 55 pouches |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00613994986467 |
| Serial numbers | 086, A57958, 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 and 31 more |
| Model numbers | 7509014 |
| Expiration dates | 2025-02-15 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2524-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.