Device recall
Z-0925-2022: Plus 30 Priority Pack w/.096 RHV - REF 1000183 WPL2122277-01 (20-03-01) Plus 30…
FDA device recall · Class II · Abbott Vascular
Key facts
| Recall number (Z-number) | Z-0925-2022 |
|---|---|
| Recall event | 89760 |
| Product | Plus 30 Priority Pack w/.096 RHV - REF 1000183 WPL2122277-01 (20-03-01) Plus 30 Priority Pack w/.115 RHV - REF 1000185-115 WPL2122279-01 (2019-03-01) |
| Product code | MAV |
| Recalling firm | Abbott Vascular |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K962495 |
| 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