Device recall
Z-2004-2016: Musculoskeletal Transplant Foundation, AFT Diverted Tube (3/4/Filled), indicated…
FDA device recall · Class II · Musculoskeletal Transplant Foundation, Inc.
Key facts
| Recall number (Z-number) | Z-2004-2016 |
|---|---|
| Recall event | 74263 |
| Product | Musculoskeletal Transplant Foundation, AFT Diverted Tube (3/4/Filled), indicated for treatment of surgically-created osseous defects or osseous defects created from traumatic injury. It can be used in the: extremities, pelvis, and spine. Product Code: 227005. |
| Product code | MBP |
| Recalling firm | Musculoskeletal Transplant Foundation, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 18, 2016 |
| 510(k) numbers | K042125, K060161 |
| FEI number | 3001236616 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database