Actavis South Atlantic LLC recalls Ranitidine Syrup (Ranitidine Oral Solution USP) 15 mg/mL, Rx Only. Manufactured by VistaPharm, Inc., Birmingham, AL 352
Recalled August 7, 2013 · FDA recall D-829-2013 · Actavis South Atlantic
Hazard
Failed Impurity/Degradation Specification; "Related Compound C" · FDA Class II
Units
A total of 133,968 bottles (units)
Sold at
Nationwide
Description
Failed Impurity/Degradation Specification; "Related Compound C"
Product
Ranitidine Syrup (Ranitidine Oral Solution USP) 15 mg/mL, Rx Only. Manufactured by VistaPharm, Inc., Birmingham, AL 35242. Distributed by Actavis Mid Atlantic LLC 1877 Kawai Road, Lincolnton, NC 28092 USA
Manufacturer(s)
Actavis South Atlantic LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →