Drug recall D-107-2013
Product
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.
Reason for recall
Labeling: Error on Declared Strength. Product labeled to contain 150 mcg tablets actually contained 75 mcg tablets.
Lots and codes
LOT # 18262A8 Exp. 09/13
Recall details
- Recalling firm
- Abbott Laboratories, Abbott Park, IL
- Quantity
- 28, 524 bottles
- Distribution
- US Nationwide and Puerto Rico
- Type
- Voluntary: Firm initiated
- Recall initiated
- December 4, 2012
- Terminated
- July 10, 2015
Related products
- Synthroid – drug information
- NDC 0074-3727 Synthroid · Levothyroxine Sodium 137 ug/1 · AbbVie Inc.
- NDC 0074-7068 Synthroid · Levothyroxine Sodium 125 ug/1 · AbbVie Inc.
- NDC 0074-4552 Synthroid · Levothyroxine Sodium 50 ug/1 · AbbVie Inc.
- NDC 0074-6624 Synthroid · Levothyroxine Sodium 100 ug/1 · AbbVie Inc.
- NDC 0074-7149 Synthroid · Levothyroxine Sodium 300 ug/1 · AbbVie Inc.
- NDC 0074-6594 Synthroid · Levothyroxine Sodium 88 ug/1 · AbbVie Inc.
- NDC 0074-9296 Synthroid · Levothyroxine Sodium 112 ug/1 · AbbVie Inc.
- NDC 0074-7070 Synthroid · Levothyroxine Sodium 175 ug/1 · AbbVie Inc.
- NDC 0074-7069 Synthroid · Levothyroxine Sodium 150 ug/1 · AbbVie Inc.
- NDC 0074-7148 Synthroid · Levothyroxine Sodium 200 ug/1 · AbbVie Inc.
- NDC 0074-5182 Synthroid · Levothyroxine Sodium 75 ug/1 · AbbVie Inc.
- NDC 0074-4341 Synthroid · Levothyroxine Sodium 25 ug/1 · AbbVie Inc.