Device recall
Z-1250-2023: Arial mobile application, model #54630 and #54640 for Android devices downloaded…
FDA device recall · Class II · Securitas Healthcare LLC
Key facts
| Recall number (Z-number) | Z-1250-2023 |
|---|---|
| Recall event | 91625 |
| Product | Arial mobile application, model #54630 and #54640 for Android devices downloaded from the Google Play Store as part of the Arial Emergency and Nurse Call system. |
| Product code | IQA |
| Recalling firm | Securitas Healthcare LLC |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1929691 |
At a glance
- None 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