Device recall
Z-0091-2007: ConMed DetachaTip Laparoscopic Instrument: Meeker (Right Angle) Multiple Use…
FDA device recall · Class II · Conmed Corporation
Key facts
| Recall number (Z-number) | Z-0091-2007 |
|---|---|
| Recall event | 36515 |
| Product | ConMed DetachaTip Laparoscopic Instrument: Meeker (Right Angle) Multiple Use Grasper, 5mm x 33cm length, REF/Product Code 1-1017. --- 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 | Aug 30, 2012 |
| 510(k) numbers | K924283 |
| FEI number | 3001451571 |
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