FDAFDA · Food and drugs·Recall number D-107-2013
Synthroid (Levothyroxine Sodium) tablets, 150 mcg (0.15 mg), 90 tablets per bottle, Rx Only, NDC 0074-7069-90; ABBOTT LABORATORIES NORTH CHICAGO, IL 60064 U.S.A.
Published January 9, 2013 · Recall initiated: December 4, 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
Labeling: Error on Declared Strength. Product labeled to contain 150 mcg tablets actually contained 75 mcg tablets.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- SYNTHROID
- Manufacturer
- Abbott Laboratories
- Distributor
- US Nationwide and Puerto Rico
- UPC
- 0300747149902
- Lot
- LOT # 18262A8 Exp. 09/13
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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