FDAFDA · Food and drugs·Recall number D-829-2013
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
Published August 7, 2013 · Recall initiated: May 15, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Impurity/Degradation Specification; "Related Compound C"
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Actavis South Atlantic LLC
- Distributor
- Nationwide
- Lot
- Lot Numbers: 247900, 251000, 256000, 261200, 263600, 266700, 277100, 280300 and 284300.
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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