Device recall
Z-1144-2010: Ascent Posterior Occipital Cervical Thoracic System, Single Looped Cable with…
FDA device recall · Class II · Blackstone Medical, Inc.
Key facts
| Recall number (Z-number) | Z-1144-2010 |
|---|---|
| Recall event | 54507 |
| Product | Ascent Posterior Occipital Cervical Thoracic System, Single Looped Cable with Two Crimps, One Each. Distributed by Blackstone Medical, Springfield, MA. Intended to promote fusion of the cervical spine and occipitothoracic junction. |
| Product code | MNI |
| Recalling firm | Blackstone Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 9, 2010 |
| 510(k) numbers | K030197 |
| FEI number | 3001238051 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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