Device recall
Z-0622-2009: Genicon 5mm Pyramidal Trocar, Sterile, Genion 6869 Stapoint Court, Suite 114…
FDA device recall · Class II · Genico, Inc., dba Genicon
Key facts
| Recall number (Z-number) | Z-0622-2009 |
|---|---|
| Recall event | 50489 |
| Product | Genicon 5mm Pyramidal Trocar, Sterile, Genion 6869 Stapoint Court, Suite 114 Winter Park, FL U.S.A. 32792, Rx Only. Catalog Numbers: 100-005-001 & 100-005-002. Used for incisions made for positioning the laparoscopic cannulas or ports. |
| Product code | GEA |
| Recalling firm | Genico, Inc., dba Genicon |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 9, 2009 |
| 510(k) numbers | K982472 |
| FEI number | 3002590791 |
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