Device recall
Z-0205-2015: Medtronic Launcher Coronary Guide Catheter; MODEL: LA6JR40K
FDA device recall · Class II · Medtronic Vascular
Key facts
| Recall number (Z-number) | Z-0205-2015 |
|---|---|
| Recall event | 69488 |
| Product | Medtronic Launcher Coronary Guide Catheter; MODEL: LA6JR40K |
| Product code | DQY |
| Recalling firm | Medtronic Vascular |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 18, 2015 |
| 510(k) numbers | K021256 |
| 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