FDAFDA · Food and drugs·Recall number D-104-2013
Levothyroxine Sodium Tablets, USP, 175 mcg in 90 ct bottles, Manufactured by Patheon Puerto Rico Inc., for Alara Pharmaceutical Corp, San Juan, PR
Published January 2, 2013 · Recall initiated: October 29, 2012
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
Subpotent; 15 month stability
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Alara Pharmaceutical Co
- Distributor
- Nationwide
- Lot
- 11T7011A, Exp. Date: 12/2012
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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