Device recall
Z-0662-2008: Tucker Embryo Catheter, Stylet, For use with Embryo Transfer Catheter, 23 CM…
FDA device recall · Class II · Fertility Technology Resources, Inc.
Key facts
| Recall number (Z-number) | Z-0662-2008 |
|---|---|
| Recall event | 45413 |
| Product | Tucker Embryo Catheter, Stylet, For use with Embryo Transfer Catheter, 23 CM, Sterile, Single Use Only, Order #: ft r 223, Manufactured by Fertility Technology Resources, Inc., Marietta, GA 30062 |
| Product code | MQF |
| Recalling firm | Fertility Technology Resources, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 6, 2008 |
| 510(k) numbers | K023017 |
| FEI number | 3003889409 |
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