RecallRadar

FDA Drug recall D-0339-2019

Levoxyl (levothyroxine sodium tablets, USP) tablets 112 mcg, 100-count bottle, Rx Only,Distributed by Pfizer Inc

On 2018-12-26 the FDA classified a Class II recall of Levoxyl (levothyroxine sodium tablets, USP) tablets 112 mcg, 100-count bottle, Rx Only,Distributed by Pfizer Inc by Pfizer, citing superpotent Drug.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0339-2019
ClassificationClass II
Statusterminated
Initiated2018-12-06
Published2018-12-26
Last updated2026-09-13 11:52 UTC
CompanyPfizer
DistributionUS

Product

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

Reason

Superpotent Drug.

Identifiers

ndc60793-850-10
ndc60793-850-01
ndc60793-851-10
ndc60793-851-01
ndc60793-852-10
ndc60793-852-01
ndc60793-853-10
ndc60793-853-01
ndc60793-854-10
ndc60793-854-01
ndc60793-855-10
ndc60793-855-01
ndc60793-856-10
ndc60793-856-01
ndc60793-857-10
ndc60793-857-01
ndc60793-858-10
ndc60793-858-01
ndc60793-859-10
ndc60793-859-01
ndc60793-860-10
ndc60793-860-01
code_infoLot #:18A18, Exp. 01/2020

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0339-2019%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.