Drug recall
DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or…
FDA recall event 93296 · Class II · Musculoskeletal Transplant Foundation, Inc.
Key facts
| Event ID | 93296 |
|---|---|
| Recall numbers | Z-0323-2024 |
| Recalling firm | Musculoskeletal Transplant Foundation, Inc. |
| Product type | Devices |
| Products | DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous defects created from traumatic injury. Model Number: 038100 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | Sep 22, 2023 |
| Report date | Nov 29, 2023 |
| City | Edison |
| State | NJ |
| Country | United States |
| FEI number | 3001236616 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: