Device recall
Z-2167-2014: Esaote PA230E Transducer A portable and cart base ultrasound system for general…
FDA device recall · Class II · Biosound Esaote, Inc.
Key facts
| Recall number (Z-number) | Z-2167-2014 |
|---|---|
| Recall event | 68648 |
| Product | Esaote PA230E Transducer A portable and cart base ultrasound system for general and cardiovascular imaging |
| Product code | JOP |
| Recalling firm | Biosound Esaote, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 17, 2015 |
| 510(k) numbers | K040596, K050326, K110688 |
| FEI number | 1826555 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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