US Drug Recall Register
Class II · Moderate risk Terminated Initiated Nov 7, 2016 (10 years ago)

LEVOXYL(R) (levothyroxine sodium tablets, USP), 200 mcg, 100 count bottles, Rx only…

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

Why it was recalled

Superpotent

What was recalled

LEVOXYL(R) (levothyroxine sodium tablets, USP), 200 mcg, 100 count bottles, Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc., Bristol, TN 37620, NDC 60793-860-01

Recalling firm
Pfizer Inc.
NDC code
60793-860-01
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0150-2017

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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