Device recall
Z-0667-2008: Morton IUI Catheter, Sterile, Single Use Only, Order #: ftr510, Manufactured by…
FDA device recall · Class II · Fertility Technology Resources, Inc.
Key facts
| Recall number (Z-number) | Z-0667-2008 |
|---|---|
| Recall event | 45413 |
| Product | Morton IUI Catheter, Sterile, Single Use Only, Order #: ftr510, 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 |
| FEI number | 3003889409 |
At a glance
- None 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