Device recall
Z-1246-2021: Medtronic 6F Launcher Guide Catheter 100 cm JR 4.0 Model Number: LA6JR40
FDA device recall · Class II · Medtronic Vascular
Key facts
| Recall number (Z-number) | Z-1246-2021 |
|---|---|
| Recall event | 87284 |
| Product | Medtronic 6F Launcher Guide Catheter 100 cm JR 4.0 Model Number: LA6JR40 |
| Product code | DQY |
| Recalling firm | Medtronic Vascular |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 15, 2023 |
| 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