Device recall
Z-1683-2014: Composix" LP with Echo PS" 6x10 Reorder Number: 0144610 Indicated for use in the…
FDA device recall · Class II · Davol, Inc., Subs. C. R. Bard, Inc.
Key facts
| Recall number (Z-number) | Z-1683-2014 |
|---|---|
| Recall event | 68124 |
| Product | Composix" LP with Echo PS" 6x10 Reorder Number: 0144610 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias. |
| Product code | GCJ |
| Recalling firm | Davol, Inc., Subs. C. R. Bard, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 23, 2015 |
| 510(k) numbers | K122436 |
| FEI number | 1213643 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 100–999 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