Device recall
Z-0819-2014: Composix L/P with Echo PS 10" X 13" Product Code 0144113 The Composix L/P Mesh…
FDA device recall · Class II · Davol, Inc., Subs. C. R. Bard, Inc.
Key facts
| Recall number (Z-number) | Z-0819-2014 |
|---|---|
| Recall event | 67149 |
| Product | Composix L/P with Echo PS 10" X 13" Product Code 0144113 The Composix L/P Mesh with Echo PS Positioning System is a non-absorbable sterile lightweight mesh prosthesis, with a preattached removable positioning system. This system is indicated and designed for the reconstruction of soft tissue… |
| Product code | FTL |
| Recalling firm | Davol, Inc., Subs. C. R. Bard, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 23, 2015 |
| 510(k) numbers | K102766 |
| 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