Data Foundry

Drug recalls 2013

Levoxyl — Class II drug recall D-257-2013

Completed recall by Pfizer Inc., reported 2013-04-24, distributed nationwide. Chemical contamination: emission of strong odor after package was opened

Recall numberD-257-2013
Product typeDrug
ClassificationClass II
StatusCompleted
Voluntary or mandatedVoluntary
Recalling firmPfizer Inc., New York, NY, United States
Recall initiated2013-03-28
Classified2013-04-18
Reported by FDA2013-04-24
DistributedNationwide (US)
Quantity37,891 bottles
Reason classeschemical contamination
NDC60793-0850, 60793-0850-01, 60793-0850-10, 60793-0851, 60793-0851-01, 60793-0851-10, 60793-0852, 60793-0852-01, 60793-0852-10, 60793-0853, 60793-0853-01, 60793-0853-10, 60793-0854, 60793-0854-01, 60793-0854-10, 60793-0855, 60793-0855-01, 60793-0855-10, 60793-0856, 60793-0856-01, 60793-0856-10, 60793-0857, 60793-0857-01, 60793-0857-10, 60793-0858 and 8 more

Product

Levoxyl (levothyroxine sodium) tablets, USP 125 mcg, packaged in a) 100-count bottles (NDC 60793-856-01) and b) 1000-count bottles ( NDC 60793-856-10 ) Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc., Bristol, TN 37620.

Reason for recall

Chemical contamination: emission of strong odor after package was opened

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-257-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.