Device recall
Z-1592-2010: Micro Introducer Kit 5F, Model number: KIT-014-29, & Customer Model number…
FDA device recall · Class II · Galt Medical Corp
Key facts
| Recall number (Z-number) | Z-1592-2010 |
|---|---|
| Recall event | 54680 |
| Product | Micro Introducer Kit 5F, Model number: KIT-014-29, & Customer Model number: 7204. Vascular Solutions, 6464 Sycamore Court, Minneapolis, MN 53369. |
| Product code | DRE |
| Recalling firm | Galt Medical Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 21, 2011 |
| 510(k) numbers | K000737 |
| FEI number | 3000718472 |
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