Device recall
Z-2349-2021: Vascular Table without Fowler (USV1) and Ultrasound Vascular Table with Fowler…
FDA device recall · Class II · Oakworks Inc
Key facts
| Recall number (Z-number) | Z-2349-2021 |
|---|---|
| Recall event | 88365 |
| Product | Vascular Table without Fowler (USV1) and Ultrasound Vascular Table with Fowler (USV2). Intended Use: Vascular Ultrasound examination table Catalog Number: 66783 and 64219 |
| Product code | LGX |
| Recalling firm | Oakworks Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 5, 2023 |
| FEI number | 1000121370 |
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