Device recall
Z-1292-2022: ProudP Everyday Uroflow Tracker Software Version 1.x.x Software Version 1.2.0 or…
FDA device recall · Class II · Dain Technology, Inc. (Subsidiary of Soundable Health, Inc.)
Key facts
| Recall number (Z-number) | Z-1292-2022 |
|---|---|
| Recall event | 90165 |
| Product | ProudP Everyday Uroflow Tracker Software Version 1.x.x Software Version 1.2.0 or earlier |
| Product code | EXY |
| Recalling firm | Dain Technology, Inc. (Subsidiary of Soundable Health, Inc.) |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 29, 2023 |
| FEI number | 3016096130 |
At a glance
- None 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