FDAFDA · Food and drugs·Recall number D-1696-2012
Synthroid (levothyroxine sodium) Tablets USP, 112 mcg, Rx Only, 90-Count Bottle, Abbott Laboratories, North Chicago, IL 60064, NDC: 0074-9296-90
Published October 3, 2012 · Recall initiated: July 19, 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
Defective Container: A number of Synthroid bottles have a localized thin wall defect on the bottom which may potentially impact the stability of the tablets.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- SYNTHROID
- Manufacturer
- Abbott Laboratories
- Distributor
- Nationwide
- UPC
- 0300747149902
- Lot
- Lot: 18355A8, Exp. 09/26/13
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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