Device recall
Z-0891-05: Peri-Strips Dry with Veritas Collagen Matrix Staple Line Reinforcement (PSD-V)…
FDA device recall · Class II · Synovis Surgical Inovation Div. of
Key facts
| Recall number (Z-number) | Z-0891-05 |
|---|---|
| Recall event | 32264 |
| Product | Peri-Strips Dry with Veritas Collagen Matrix Staple Line Reinforcement (PSD-V), 4506 ETS-V. PSD-V is an implantable surgical mesh comprised of non-crosslinked bovine pericardium in a dehydrated form. Do not reuse. Consult Instructions for Use. Sterilized. Product treated with sodium hydroxide… |
| Product code | FTM |
| Recalling firm | Synovis Surgical Inovation Div. of |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 17, 2005 |
| 510(k) numbers | K041699 |
| 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