Device recall
Z-1081-2007: Allez Medical Applications, Inc. 4Closure Surgical Fascia Closure System…
FDA device recall · Class II · Synovis Surgical Inovation Div. of
Key facts
| Recall number (Z-number) | Z-1081-2007 |
|---|---|
| Recall event | 38261 |
| Product | Allez Medical Applications, Inc. 4Closure Surgical Fascia Closure System , Catalgo ref. 4-12GPS. Sterile, One Time Use, Contents 4 sets 1- suture passer instrument, 1-guide rod, 12mm, 250 mm long. Distributed by Aliez Medical Applications, Inc., Santa Ana, CA 92707. Synovis over labels the… |
| Product code | GDF |
| Recalling firm | Synovis Surgical Inovation Div. of |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 8, 2012 |
| FEI number | 2183620 |
At a glance
- None 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