Device recall
Z-0609-2013: Diamigo i-Phone App The Diamigo app was intended for use as an educational tool…
FDA device recall · Class II · sanofi-aventis US, Inc.
Key facts
| Recall number (Z-number) | Z-0609-2013 |
|---|---|
| Recall event | 63803 |
| Product | Diamigo i-Phone App The Diamigo app was intended for use as an educational tool in the management of diabetes. |
| Recalling firm | sanofi-aventis US, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 22, 2015 |
| FEI number | 2222017 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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