Device recall
Z-0770-2007: 83 plus Mini-flex with accessory crate, Custom Ultrasonics, Inc.
FDA device recall · Class II · Custom Ultrasonics, Inc.
Key facts
| Recall number (Z-number) | Z-0770-2007 |
|---|---|
| Recall event | 37702 |
| Product | 83 plus Mini-flex with accessory crate, Custom Ultrasonics, Inc. |
| Product code | FEB |
| Recalling firm | Custom Ultrasonics, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 20, 2013 |
| 510(k) numbers | K061430 |
| FEI number | 2523209 |
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