Device recall
Z-2316-2024: GE Vivid Ultrasound products, Model Numbers: a) Vivid E90, H45581LB; b) Vivid…
FDA device recall · Class II · GE Vingmed Ultrasound As
Key facts
| Recall number (Z-number) | Z-2316-2024 |
|---|---|
| Recall event | 94772 |
| Product | GE Vivid Ultrasound products, Model Numbers: a) Vivid E90, H45581LB; b) Vivid E95, H45581DA |
| Product code | IYN |
| Recalling firm | GE Vingmed Ultrasound As |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K150087 |
| FEI number | 3002808457 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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