Data Foundry

Drug recalls 2017

Fluocinonide Cream UPS — Class III drug recall D-0790-2017

Terminated recall by Taro Pharmaceuticals U.S.A., Inc., reported 2017-05-24, distributed nationwide. Cross contamination with other products: Certain lots of Fluocinonide Cream were found to be contaminated with

Recall numberD-0790-2017
Product typeDrug
ClassificationClass III
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmTaro Pharmaceuticals U.S.A., Inc., Hawthorne, NY, United States
Recall initiated2017-03-17
Classified2017-05-18
Reported by FDA2017-05-24
Terminated2021-08-24
DistributedNationwide (US)
Quantity7,776 tubes
NDC51672-1253, 51672-1253-01, 51672-1253-02, 51672-1253-03, 51672-1253-04, 51672-1254, 51672-1254-01, 51672-1254-02, 51672-1254-03, 51672-1264, 51672-1264-01, 51672-1264-02, 51672-1264-03, 51672-1279, 51672-1279-01, 51672-1279-02, 51672-1279-03
Lot numbersD301311473, D301411473
Expiration dates2017-03

Product

Fluocinonide Cream UPS, 0.05% (Emulsified Base), packaged in 60 g tube, Rx only, Mfd. by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada, Dist. by Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532, NDC 51672-1254-3

Reason for recall

Cross contamination with other products: Certain lots of Fluocinonide Cream were found to be contaminated with a small quantity of hydrocortisone-17-valerate.

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-0790-2017. 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.