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Lower risk Drug recall · FDA · Published March 17, 2017

Taro Fluocinonide Cream 0.05% Recall: Cross Contamination Risk

Taro Pharmaceuticals recalls certain lots of Fluocinonide Cream 0.05% (60g tube) due to cross contamination with hydrocortisone-17-valerate. This may cause unintended medication effects. Contact Taro for details.

🇺🇸 FDA recall #D-0790-2017DrugTaro Pharmaceuticals ›
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Recalling firmTaro Pharmaceuticals U.S.A., Inc.3 Skyline Dr · Hawthorne, NY 10532-2174
✎ GovInfoNow plain-language explainer

What happened, in plain English

Taro Pharmaceuticals is recalling specific lots of Fluocinonide Cream 0.05% (60g tube) because some batches were contaminated with hydrocortisone-17-valerate. This cross-contamination could lead to unintended medication effects if used without proper medical guidance. Read more at govinfonow.com/recall/41806-taro-fluocinonide-cream-0-05-recall-cross-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/41806-taro-fluocinonide-cream-0-05-recall-cross-contamination-risk · Updated October 8, 2026 · FDA enforcement record: FDA #D-0790-2017

Cite this page

“Taro Fluocinonide Cream 0.05% Recall: Cross Contamination Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/41806-taro-fluocinonide-cream-0-05-recall-cross-contamination-risk. Based on FDA recall #D-0790-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0790-2017%22&limit=1).

Why it’s dangerous

The cream was found to contain a small amount of hydrocortisone-17-valerate, a different corticosteroid. This cross-contamination could cause unintended medication effects if the product is used without proper medical guidance.

Who’s affected

People with prescriptions for Fluocinonide Cream 0.05% (60g tube) from the recalled lots. Those using the product without medical supervision are at higher risk of unintended medication effects.

How to tell if you have this one

Check for the product name 'Fluocinonide Cream UPS, 0.05% (Emulsified Base)', 60g tube, prescription-only. Look for lot numbers D301311473 or D301411473 with expiration date 3/2017.

  • Brand
    Taro Pharmaceuticals
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Identify if your product matches the recalled description: Fluocinonide Cream 0.05% (60g tube), prescription-only, with lot numbers D301311473 or D301411473.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “U.S. Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 4.4 years after the firm started it.

1. Firm started the recall: Mar 17, 201712. FDA classified it Class III: May 18, 201723. Published in FDA’s Enforcement Report: May 24, 201734. FDA terminated the recall: Aug 24, 2021420172021
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0790-2017 (March 17, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0790-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 8, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA