Device recall
Z-2178-2008: Flexipet Manipulation Pipette 300 micron. The product is boxed with 1 vial of 10…
FDA device recall · Class II · Cook Vascular Inc.
Key facts
| Recall number (Z-number) | Z-2178-2008 |
|---|---|
| Recall event | 48630 |
| Product | Flexipet Manipulation Pipette 300 micron. The product is boxed with 1 vial of 10 pipettes. This product 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 16, 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