DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of… — Class II medical device recall Z-0323-2024
Ongoing recall by Musculoskeletal Transplant Foundation, Inc., reported 2023-11-29, distributed nationwide. Units are labeled as 10cc; however the units have a fill volume of 1cc units. This may result in prolongation
| Recall number | Z-0323-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Musculoskeletal Transplant Foundation, Inc., Edison, NJ, United States |
| Recall initiated | 2023-09-22 |
| Classified | 2023-11-17 |
| Reported by FDA | 2023-11-29 |
| Distributed | Nationwide (US) |
| Quantity | 18 units |
| Reason classes | labeling |
| Serial numbers | 002220854711400001, 002220854711400002, 002220854711400003, 002220854711400004, 002220854711400005, 002220854711400006, 002220854711400007, 002220854711400008, 002220854711400009, 002220854711400010, 002220854711400011, 002220854711400012, 002220854711400013, 002220854711400014, 002220854711400056 |
| Model numbers | 038100 |
| Expiration dates | 2025-06-20 |
Product
DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous defects created from traumatic injury. Model Number: 038100
Reason for recall
Units are labeled as 10cc; however the units have a fill volume of 1cc units. This may result in prolongation of surgery.
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-0323-2024. 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.