sanofi-aventis US recalls

sanofi-aventis US has 3 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 2 Jan 2013. The most frequent reason is manufacturing (cgmp) deviations.

Total recalls3since 2012

Last 12 months0reported

Class I00% of total

Ongoing0latest 2 Jan 2013

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 3 100%Class III 0 0%

Why sanofi-aventis us is recalled

Manufacturing (CGMP) Deviations267%
Device Malfunction133%

Product types

Injectable & IV Drugs267%
Medical Software133%

By year

2013133%
2012267%

All sanofi-aventis us recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
2 Jan 2013Device	CLASS II	Diamigo i-Phone App The Diamigo app was intended recalled	sanofi-aventis US	Device Malfunction	NJ
11 Jul 2012Drug	CLASS II	Eloxatin (OXALIplatin injection) 5 mg/mL injection, 100 mg recalled	sanofi-aventis US	Manufacturing (CGMP) Deviations	Nationwide
11 Jul 2012Drug	CLASS II	Eloxatin (OXALIplatin injection) 5 mg/mL Injection, 50 mg recalled	sanofi-aventis US	Manufacturing (CGMP) Deviations	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.