FDA Drugs recall ·
Levoxyl (levothyroxine sodium tablets, USP), tablets, 175 mcg… recall
Read the official FDA notice ↗
Product
Levoxyl (levothyroxine sodium tablets, USP), tablets, 175 mcg, 1000-count bottle, Rx only, Distributed by Pfizer Inc., New York, NY 10017, Made in Austria. NDC 60793-859-10
Why was it recalled?
Subpotent Drug: confirmed out-of-specification (OOS) assay during stability testing.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot # 24W07, Exp: 11/30/2026
Distribution
US Nationwide and Puerto Rico
States: Puerto Rico
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (drugs), recall D-0051-2027. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.