Device recall
Z-1249-2016: Reveal LINQ insertable Cardiac Monitor, Model LNQ11. Monitors subcutaneous ECG…
FDA device recall · Class II · Medtronic Inc.
Key facts
| Recall number (Z-number) | Z-1249-2016 |
|---|---|
| Recall event | 73494 |
| Product | Reveal LINQ insertable Cardiac Monitor, Model LNQ11. Monitors subcutaneous ECG continuously. |
| Product code | DSI |
| Recalling firm | Medtronic Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 25, 2017 |
| 510(k) numbers | K132649 |
| FEI number | 2182208 |
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