Device recall
Z-1485-2017: PureWick External Catheter for Women-Wick Product Usage: A flexible, contoured…
FDA device recall · Class II · Purewick Corporation
Key facts
| Recall number (Z-number) | Z-1485-2017 |
|---|---|
| Recall event | 76571 |
| Product | PureWick External Catheter for Women-Wick Product Usage: A flexible, contoured external catheter (a Wick) is positioned between the labia and gluteus muscles. The function of the Wick is to draw urine away from the body through the Wick to a storage container away from the body through a PVC tube… |
| Product code | NNW |
| Recalling firm | Purewick Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 9, 2017 |
| FEI number | 3012224959 |
At a glance
- None 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