Synthroid: 5 recalls on record

Recalled by 1 agency: FDA (5).

First recall on record: October 3, 2012. Most recent: November 15, 2023.

Risk classification: Class II: 4 · Class III: 1

Most recent recalls

DateAgencyProduct
November 15, 2023FDASynthroid, Levothyroxine Sodium Tablets, USP 125mcg (0.125mg), 100-count bottle, Rx Only …D-0088-2024
January 9, 2013FDASynthroid (Levothyroxine Sodium) tablets, 150 mcg (0.15 mg), 90 tablets per bottle, Rx On…D-107-2013
October 3, 2012FDASynthroid (levothyroxine sodium) Tablets USP, 112 mcg, Rx Only, 90-Count Bottle, Abbott L…D-1696-2012
October 3, 2012FDASynthroid (levothyroxine sodium) Tablets USP, 75 mcg, Rx Only, 90-Count Bottle, Abbott La…D-1695-2012
October 3, 2012FDASynthroid (levothyroxine sodium) Tablets USP, 50 mcg, Rx Only, 90-Count Bottle, Abbott La…D-1694-2012

Questions about this brand

How many recalls does Synthroid have?
Recalert has 5 U.S. recalls on record for Synthroid, published between October 3, 2012 and November 15, 2023.
What was the most recent Synthroid recall?
FDA recall D-0088-2024, published November 15, 2023: Synthroid, Levothyroxine Sodium Tablets, USP 125mcg (0.125mg), 100-count bottle, Rx Only AbbVie Inc. North Chicago, IL 60064, U.S.A. NDC 0074-7068-11
Which agencies have recalled Synthroid products?
Synthroid products appear in recalls from: FDA (5).

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