Device recall
Z-2620-2016: Aprima Access Nonvascular Introducer Set Accessories, Catheter Intended for…
FDA device recall · Class II · Cook Inc.
Key facts
| Recall number (Z-number) | Z-2620-2016 |
|---|---|
| Recall event | 74010 |
| Product | Aprima Access Nonvascular Introducer Set Accessories, Catheter Intended for single-puncture percutaneous access to facilitate placement of an .038 inch (0.97 mm) diameter working wire guide for interventional radiology procedures |
| Product code | KGZ |
| Recalling firm | Cook Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 4, 2017 |
| FEI number | 1820334 |
At a glance
- None Linked 510(k)s
- 10–99 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