FDA Device recall Z-0609-2013
Diamigo i-Phone App The Diamigo app was intended for use as an educational tool in the management of diabetes
- FDA Device
- Class II
- terminated
- Published 2013-01-02
On 2013-01-02 the FDA classified a Class II recall of Diamigo i-Phone App The Diamigo app was intended for use as an educational tool in the management of diabetes by Sanofi Aventis Us, citing diamigo, a software application, was released through the i-Phone Global Store which inadvertently allowed global access to the application as opposed to the original intended res….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0609-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-09-21 |
| Published | 2013-01-02 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Sanofi Aventis Us |
| Distribution | n/a |
Product
Diamigo i-Phone App The Diamigo app was intended for use as an educational tool in the management of diabetes.
Reason
Diamigo, a software application, was released through the i-Phone Global Store which inadvertently allowed global access to the application as opposed to the original intended restriction of access to Brazil.
Identifiers
| code_info | n/a |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0609-2013%22
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