Device recall
Z-1793-2008: Lamis Tubing Set, 9'; 10/box; Part Number LAM-TUBING; distributed by Mentor…
FDA device recall · Class II · Mentor Texas, Inc
Key facts
| Recall number (Z-number) | Z-1793-2008 |
|---|---|
| Recall event | 47873 |
| Product | Lamis Tubing Set, 9'; 10/box; Part Number LAM-TUBING; distributed by Mentor Texas, LP, Irving, TX 75038. |
| Product code | FPK |
| Recalling firm | Mentor Texas, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 29, 2010 |
| FEI number | 1000118360 |
At a glance
- None Linked 510(k)s
- 10–99 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