Device recall
Z-0727-2024: Ultrasound EA (Ergonomic Advantage) table versions; G2 (GENERAL 2) -An…
FDA device recall · Class II · Oakworks Inc
Key facts
| Recall number (Z-number) | Z-0727-2024 |
|---|---|
| Recall event | 93595 |
| Product | Ultrasound EA (Ergonomic Advantage) table versions; G2 (GENERAL 2) -An Ultrasound examination table |
| Product code | LGX |
| Recalling firm | Oakworks Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 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