US Drug Recall Register
Class II · Moderate risk Terminated Initiated Dec 6, 2018 (8 years ago)

Levoxyl (levothyroxine sodium tablets, USP) tablets 112 mcg, 100-count bottle, Rx…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Superpotent Drug.

What was recalled

Levoxyl (levothyroxine sodium tablets, USP) tablets 112 mcg, 100-count bottle, Rx Only,Distributed by Pfizer Inc. New York, NY 10017, NDC 60793-855-01

Recalling firm
Pfizer Inc.
NDC code
60793-855-01
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0339-2019

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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