Device recall
Z-2754-2011: Medtronic 6F Zuma Guide Catheter with AL 1.5 Curve with side holes Catalog…
FDA device recall · Class II · Medtronic Vascular
Key facts
| Recall number (Z-number) | Z-2754-2011 |
|---|---|
| Recall event | 59111 |
| Product | Medtronic 6F Zuma Guide Catheter with AL 1.5 Curve with side holes Catalog Number: Z26AL15SH The Medtronic Guiding Catheter is designed to provide a pathway through which therapeutic devices are introduced. The guiding catheter is intended to be used in the coronary or peripheral vascular system. |
| Product code | DQY |
| Recalling firm | Medtronic Vascular |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 17, 2012 |
| 510(k) numbers | K010579, K990707 |
| FEI number | 1220452 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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