Device recall
Z-2176-2008: Flexipet Denuding pipette 130 micron. The product is boxed with 5 vials of 10…
FDA device recall · Class II · Cook Vascular Inc.
Key facts
| Recall number (Z-number) | Z-2176-2008 |
|---|---|
| Recall event | 48629 |
| Product | Flexipet Denuding pipette 130 micron. The product is boxed with 5 vials of 10. The device is used for the intracytoplasmic single sperm injection of oocytes. |
| Product code | MQH |
| Recalling firm | Cook Vascular Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 18, 2008 |
| 510(k) numbers | K983596 |
| FEI number | 2522007 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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