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Drug recall · FDA · Published December 21, 2017

Taro Pharmaceuticals U.S.A., Inc. recalls Clobetasol Propionate Cream USP, 0.05% 60 g tube, Rx only Mfd. by: Taro Pharmaceutical Industries Ltd., Haifa Bay,

Taro Pharmaceuticals recalls 0.05% Clobetasol Propionate Cream tubes due to failed content uniformity. This may affect medication accuracy. Check your product details to see if you are affected.

🇺🇸 FDA recall #D-0249-2018DrugTaro ›
Take action

Contact the company & request your remedy

Recalling firmTaro Pharmaceuticals U.S.A., Inc.3 Skyline Dr · Hawthorne, NY 10532-2174
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
✎ GovInfoNow plain-language explainer

What happened, in plain English

Taro Pharmaceuticals is recalling 0.05% Clobetasol Propionate Cream tubes because they failed content uniformity tests. This means the medication might not deliver the correct dose, which could lead to treatment issues. Read more at govinfonow.com/recall/41004-taro-clobetasol-cream-recall-failed-content-uniformity.

Source Summary by GovInfoNow · govinfonow.com/recall/41004-taro-clobetasol-cream-recall-failed-content-uniformity · Updated October 7, 2026 · FDA enforcement record: FDA #D-0249-2018

Cite this page

“Taro Clobetasol Cream Recall: Failed Content Uniformity.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/41004-taro-clobetasol-cream-recall-failed-content-uniformity. Based on FDA recall #D-0249-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0249-2018%22&limit=1).

Why it’s dangerous

The cream failed content uniformity tests, meaning the actual medication concentration might be different from what's labeled. This could result in inconsistent treatment effectiveness, but it doesn't cause immediate harm or injury.

Who’s affected

People with a prescription for this cream, especially those using it for skin conditions like eczema or psoriasis. Those who have been using the product without a doctor's supervision are not affected since it's prescription-only.

How to tell if you have this one

Check for the product name 'Clobetasol Propionate Cream USP, 0.05% 60 g tube' with the lot number 311235 and expiration date September 2018. The product is prescription-only and distributed by Taro Pharmaceuticals U.S.A., Inc.

  • Brand
    Taro
  • Product
    Clobetasol Propionate Cream USP, 0.05% 60 g tube, Rx only Mfd. by: Taro Pharmaceutical Industries Ltd., Haifa Bay
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the lot number 311235 and expiration date September 2018 on the tube.

✎ GovInfoNow

Questions people ask

Is this cream safe to use?

The recall is due to failed content uniformity tests, which may affect medication accuracy but does not cause immediate harm. Consult your doctor for advice.

How do I know if I have the recalled product?

Check for the lot number 311235 and expiration date September 2018 on the tube. The product is prescription-only and distributed by Taro Pharmaceuticals U.S.A., Inc.

What should I do if I have the recalled product?

The recall does not require immediate action. Check the product details and contact your doctor for guidance on whether to continue using it.

Take action

Contact Taro

We’ve drafted a message you can send Taro to request your refund or repair — edit it as you like.

Subject: Recall D-0249-2018 — Taro Clobetasol Propionate Cream USP, 0.05% 60 g tube, Rx only Mfd. by: Taro Pharmaceutical Industr

Hello,

I own a Clobetasol Propionate Cream USP, 0.05% 60 g tube, Rx only Mfd. by: Taro Pharmaceutical Industries Ltd., Haifa Bay that is covered by recall D-0249-2018 from Taro.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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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-0249-2018 (December 21, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0249-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 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