Device recall
Z-0353-2020: 2000 Vascular with 30 Degree option
FDA device recall · Class II · Heritage Medical Products, Inc.
Key facts
| Recall number (Z-number) | Z-0353-2020 |
|---|---|
| Recall event | 83219 |
| Product | 2000 Vascular with 30 Degree option |
| Product code | LGX |
| Recalling firm | Heritage Medical Products, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 14, 2020 |
| FEI number | 3003881889 |
At a glance
- None 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