Drug recall D-1696-2012
Product
Synthroid (levothyroxine sodium) Tablets USP, 112 mcg, Rx Only, 90-Count Bottle, Abbott Laboratories, North Chicago, IL 60064, NDC: 0074-9296-90
Reason for recall
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.
Lots and codes
Lot: 18355A8, Exp. 09/26/13
Recall details
- Recalling firm
- Abbott Laboratories, Abbott Park, IL
- Quantity
- 40,464 Bottles
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- July 19, 2012
- Terminated
- November 1, 2013
Related products
- Synthroid – drug information
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