Device recall
Z-0764-06: Peri-Strips Dry with Veritas Collagen Matrix Circular Staple Line Reinforcement…
FDA device recall · Class II · Synovis Surgical Inovation Div. of
Key facts
| Recall number (Z-number) | Z-0764-06 |
|---|---|
| Recall event | 34052 |
| Product | Peri-Strips Dry with Veritas Collagen Matrix Circular Staple Line Reinforcement. Do not reuse. Ethylene Oxide Sterilized. Made in the U.S.A. Synovis Surgical Innovations A division of Synovis Life Technologies, Inc., 2575 University Ave. W., St. Paul, MN 55114-1024 USA. |
| Product code | FTM |
| Recalling firm | Synovis Surgical Inovation Div. of |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 3, 2007 |
| 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