Sanofi Aventis U.S., LLC
Country not established
- Devices
- 1
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Bryrel Syrup Ref N17796
Regimes: PMA, withdrawn Registry: PMA
FDA recalls
2012
- 21 Sep 2012 Z-0609-2013 Class II Terminated 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.
Frequently asked questions
How many devices does Sanofi Aventis U.S., LLC have in the registry?
The registry currently lists 1 device for Sanofi Aventis U.S., LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sanofi Aventis U.S., LLC's devices?
Among its 1 most recently registered device, Sanofi Aventis U.S., LLC has devices listed in FDA PMA (1 device).
Are there FDA recall records for Sanofi Aventis U.S., LLC?
FDA recall records list 1 recall initiated by Sanofi Aventis U.S., LLC, the most recent initiated on 21 Sep 2012. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Sanofi Aventis U.S., LLC in the registry?
The most recently registered devices listed for Sanofi Aventis U.S., LLC include BRYREL SYRUP.