Device recall
Z-0191-2015: Bard PerFix Light Plug The Bard PerFix Light Plug is indicated for reinforcement…
FDA device recall · Class II · Davol, Inc., Subs. C. R. Bard, Inc.
Key facts
| Recall number (Z-number) | Z-0191-2015 |
|---|---|
| Recall event | 69464 |
| Product | Bard PerFix Light Plug The Bard PerFix Light Plug is indicated for reinforcement if soft tissue, where weakness exists, in procedures involving soft tissue repair, such as groin hernia defects. |
| 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 | K092032 |
| 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