Device recall
Z-2412-2012: Bard Ventralight ST Mesh. - Ellipse 8" x 10" (20.3 cm x 25.4 cm) Product Code…
FDA device recall · Class II · Davol, Inc., Subs. C. R. Bard, Inc.
Key facts
| Recall number (Z-number) | Z-2412-2012 |
|---|---|
| Recall event | 63069 |
| Product | Bard Ventralight ST Mesh. - Ellipse 8" x 10" (20.3 cm x 25.4 cm) Product Code 5954810. The Bard Ventralight ST Mesh is a dual-component (absorbable and nonabsorbable) sterile prosthesis. The device classification name is "Mesh, Surgical, Polymeric." It is in tented for use in the reconstruction of… |
| Product code | FTL |
| Recalling firm | Davol, Inc., Subs. C. R. Bard, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 3, 2013 |
| 510(k) numbers | K101851 |
| FEI number | 1213643 |
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