Device recall
Z-1307-2009: Hydrophilic Guidewire, Catalog Number: VM18352,.035/150 cm…
FDA device recall · Class II · Argon Medical Devices, Inc
Key facts
| Recall number (Z-number) | Z-1307-2009 |
|---|---|
| Recall event | 51284 |
| Product | Hydrophilic Guidewire, Catalog Number: VM18352, .035/150 cm, regular/angled/standard, sold as a single hydrophilic guidewire in sterile packaging. VisioMed International Group Inc., 14555 South Robert Trail - #208, Rosemount, MN 55068, www.visiomedical.com. |
| Product code | DQX |
| Recalling firm | Argon Medical Devices, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 7, 2010 |
| 510(k) numbers | K011905 |
| FEI number | 1625425 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 100–999 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