Device recall
Z-0274-2012: Peri-Strips Dry with Veritas Collagen Matrix Staple Line Reinforcement (PSDV)…
FDA device recall · Class III · Synovis Surgical Inovation Div. of
Key facts
| Recall number (Z-number) | Z-0274-2012 |
|---|---|
| Recall event | 60328 |
| Product | Peri-Strips Dry with Veritas Collagen Matrix Staple Line Reinforcement (PSDV), sterile EO, Rx Only, Synovis Surgical Innovations, A Division of Synovis Life Technologies, Inc, 2575 University Ave W., St Paul, MN 55114-1024. The device is intended to be used as a staple line buttress |
| Product code | FTM |
| Recalling firm | Synovis Surgical Inovation Div. of |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 24, 2012 |
| 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