Device recall
Z-0112-2021: Langston Dual Lumen Catheter.
FDA device recall · Class I · Vascular Solutions, Inc.
Key facts
| Recall number (Z-number) | Z-0112-2021 |
|---|---|
| Recall event | 86433 |
| Product | Langston Dual Lumen Catheter. |
| Product code | DQO |
| Recalling firm | Vascular Solutions, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 18, 2024 |
| 510(k) numbers | K051395 |
| FEI number | 3002827704 |
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