Device recall
Z-1433-06: ConMed DetachaTip Multi-Use Laparoscopic Instrument - "Fenestrated (Duckbill)…
FDA device recall · Class II · Conmed Corporation
Key facts
| Recall number (Z-number) | Z-1433-06 |
|---|---|
| Recall event | 35949 |
| Product | ConMed DetachaTip Multi-Use Laparoscopic Instrument - "Fenestrated (Duckbill) Multiple Use Grasper", 5 mm x 33 cm, REF/Product code-1-1008. ------- The product is distributed sterile in heat-sealed tray and labeled with an expiration date that pertains only to the sterility. |
| Product code | GEI |
| Recalling firm | Conmed Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 27, 2012 |
| 510(k) numbers | K924283 |
| FEI number | 3001451571 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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