Device recall
Z-2603-2016: TIGR Matrix Surgical Mesh, Model No. NSTM1015, NSTM1520, NSTM2030
FDA device recall · Class II · Novus Scientific Ab
Key facts
| Recall number (Z-number) | Z-2603-2016 |
|---|---|
| Recall event | 74801 |
| Product | TIGR Matrix Surgical Mesh, Model No. NSTM1015, NSTM1520, NSTM2030 |
| Product code | FTL |
| Recalling firm | Novus Scientific Ab |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 23, 2016 |
| 510(k) numbers | K092224 |
| FEI number | 3010187263 |
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