Device recall
Z-2360-2019: DOSI-FUSER 12591 5-500D1 -USA, 12591 5-600D1 -USA Provide parenteral drug…
FDA device recall · Class II · Leventon S. A. U.
Key facts
| Recall number (Z-number) | Z-2360-2019 |
|---|---|
| Recall event | 83017 |
| Product | DOSI-FUSER 12591 5-500D1 -USA, 12591 5-600D1 -USA Provide parenteral drug infusions at a constant flow without impeding patient mobility |
| Product code | MEB |
| Recalling firm | Leventon S. A. U. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 8, 2020 |
| FEI number | 3002807471 |
At a glance
- None 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