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.
Reported: January 9, 2013 Initiated: December 4, 2012 #D-107-2013
Product Description
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.
Details
- Recalling Firm
- Abbott Laboratories
- Units Affected
- 28, 524 bottles
- Distribution
- US Nationwide and Puerto Rico
- Location
- Abbott Park, IL
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Abbott Laboratories. Units affected: 28, 524 bottles.
Why was this product recalled? ▼
Labeling: Error on Declared Strength. Product labeled to contain 150 mcg tablets actually contained 75 mcg tablets.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on January 9, 2013. Severity: Moderate. Recall number: D-107-2013.
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