Device recall
Z-2107-2013: SpineNet Bone Marrow Aspiration Needle Kit (which is the Ranfac Bone Marrow…
FDA device recall · Class II · SpineNet
Key facts
| Recall number (Z-number) | Z-2107-2013 |
|---|---|
| Recall event | 65914 |
| Product | SpineNet Bone Marrow Aspiration Needle Kit (which is the Ranfac Bone Marrow Aspiration Needle #74150-01M). Use to aspirate bone morrow. |
| Product code | GAA |
| Recalling firm | SpineNet |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 15, 2013 |
| FEI number | 3006755626 |
At a glance
- None 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