Device recall
Z-0464-2022: Instructions for Use for all model numbers of the Medtronic Abre Venous…
FDA device recall · Class II · Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Key facts
| Recall number (Z-number) | Z-0464-2022 |
|---|---|
| Recall event | 89140 |
| Product | Instructions for Use for all model numbers of the Medtronic Abre Venous Self-Expanding Stent System. |
| Product code | QAN |
| Recalling firm | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 16, 2024 |
| PMA numbers | P200026 |
| FEI number | 2182208 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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