Device recall
Z-0731-2025: 20/30 Priority Pack Accessory Kit/.096 RHV, REF: 1000186, or use during vascular…
FDA device recall · Class II · Abbott Vascular Inc
Key facts
| Recall number (Z-number) | Z-0731-2025 |
|---|---|
| Recall event | 95707 |
| Product | 20/30 Priority Pack Accessory Kit/.096 RHV, REF: 1000186, or use during vascular procedures in conjunction with interventional and / or diagnostic devices (e.g., balloon dilatation catheters, atherectomy devices, stent delivery systems, intravascular ultrasound devices). |
| Product code | MAV |
| Recalling firm | Abbott Vascular Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K961471 |
| FEI number | 2024168 |
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