Device recall
Z-0148-2008: Ellex, Eye Cubed, I 3 System-ABD Ultrasound Version 3.0 with Software Version…
FDA device recall · Class II · Ellex Inc.
Key facts
| Recall number (Z-number) | Z-0148-2008 |
|---|---|
| Recall event | 45398 |
| Product | Ellex, Eye Cubed, I 3 System-ABD Ultrasound Version 3.0 with Software Version 3.0 and Biometry A-scan modality, Ellex Innovative Imaging, Sacramento, CA 95827 |
| Product code | IYO |
| Recalling firm | Ellex Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 8, 2008 |
| 510(k) numbers | K041947 |
| FEI number | 1000123964 |
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