Device recall
Z-0960-2007: Synovis Peri-Strips Dry with Veritas Collagen Matrix Circular Staple Line…
FDA device recall · Class II · Synovis Surgical Inovation Div. of
Key facts
| Recall number (Z-number) | Z-0960-2007 |
|---|---|
| Recall event | 37671 |
| Product | Synovis Peri-Strips Dry with Veritas Collagen Matrix Circular Staple Line Reinforcement,( PSD 21-E-V), 21mm, Ethicon Circular stapler. Each package contains the following components: Cartridge and anvil assemblies, Cartridge cone, PSD Gel, & C-clip. |
| Product code | FTM |
| Recalling firm | Synovis Surgical Inovation Div. of |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 24, 2008 |
| 510(k) numbers | K041669 |
| FEI number | 2183620 |
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