Device recall
Z-2124-2011: BardVentralex" Hernia Patch Medium Circle with Strap Diameter 6.4cm /2.5",\…
FDA device recall · Class II · Davol, Inc., Sub. C. R. Bard, Inc.
Key facts
| Recall number (Z-number) | Z-2124-2011 |
|---|---|
| Recall event | 58470 |
| Product | BardVentralex" Hernia Patch Medium Circle with Strap Diameter 6.4cm /2.5",\ Catalog #0010302, lot number HUTL1283. The BardVentralex" Hernia Patch is a self-expanding, non-absorbable, sterile prosthesis. The device classification name is "Mesh, Surgical, Polymeric". It is intended for use in all… |
| Product code | FTL |
| Recalling firm | Davol, Inc., Sub. C. R. Bard, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 27, 2011 |
| 510(k) numbers | K021736 |
| 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