Device recall
Z-1098-2026: Abre Venous Self-Expanding Stent System, Model numbers AB9G14120090 AB9G12100090…
FDA device recall · Class II · Medtronic Inc
Key facts
| Recall number (Z-number) | Z-1098-2026 |
|---|---|
| Recall event | 98157 |
| Product | Abre Venous Self-Expanding Stent System, Model numbers AB9G14120090 AB9G12100090 AB9G14080090 AB9G12080090 AB9U12060090 AB9U14100090 AB9U14080090 AB9U12080090 AB9U14060090 AB9G14100090 AB9G12060090 |
| Product code | QAN |
| Recalling firm | Medtronic Inc |
| Recall class | Class II |
| Status | Open, Classified |
| PMA numbers | P200026 |
| FEI number | 2183870 |
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