Device recall
Z-2299-2020: Triever20 Aspiration Guide Catheter a component of FlowTriever Retrieval/…
FDA device recall · Class II · INARI MEDICAL
Key facts
| Recall number (Z-number) | Z-2299-2020 |
|---|---|
| Recall event | 85424 |
| Product | Triever20 Aspiration Guide Catheter a component of FlowTriever Retrieval/ Aspiration System, UDI: 00850291007079 |
| Product code | DXE |
| Recalling firm | INARI MEDICAL |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 13, 2021 |
| 510(k) numbers | K182233 |
| FEI number | 3011525976 |
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