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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Drug
Medications & Supplements/Topical Products

Lucky Mart Inc.: PIYANPING Anti-Itch Lotion Recalled for Containing Incorrect Drug Ingredient

Agency Publication Date: October 24, 2017
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Summary

Lucky Mart Inc. is recalling approximately 13,800 tubes of PIYANPING Anti-Itch (hydrocortisone) Lotion, 1%, because the product was manufactured with the incorrect drug formulation. Instead of the intended hydrocortisone, the product actually contains dexamethasone. This recall affects 0.67 oz (20g) tubes distributed nationwide across the United States. Consumers should stop using the product immediately as it contains a more potent corticosteroid than labeled.

Risk

Using a product containing dexamethasone instead of hydrocortisone may cause unexpected side effects or medical complications because dexamethasone is significantly more potent. If applied to large areas or for long periods, it can lead to serious health issues including high blood sugar, hormonal imbalances, or skin thinning.

What You Should Do

  1. Check your medicine cabinet for PIYANPING Anti-Itch (hydrocortisone) Lotion, 1% in a 0.67 oz (20g) tube.
  2. Identify if your product is affected by looking for Lot numbers C16001 or C16002 with an expiration date of 12/18 (December 2018) printed on the packaging.
  3. Verify the NDC number 68085-8012-4 is present on the tube or box.
  4. Immediately stop using any affected lotion and contact your healthcare provider or pharmacist for guidance regarding the use of this product.
  5. Return any unused tubes of the recalled lotion to the place of purchase for a full refund.
  6. Contact the distributor, Lucky Mart Inc., at 2210 N Seaman Ave, South El Monte, California, 91733 for further instructions regarding this recall.
  7. Contact the FDA Consumer Complaint hotline for additional questions at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Drug recall baseline remedy

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: PIYANPING Anti-Itch (hydrocortisone) Lotion, 1% (0.67 oz/20g tube)
Model:
NDC 68085-8012-4
Recall #: D-0031-2018
Lot Numbers:
C16001 (Exp 12/18)
C16002 (Exp 12/18)
Date Ranges: Expiration Date 12/18

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 78051
Status: Resolved
Manufacturer: Lucky Mart Inc.
Sold By: Lucky Mart
Manufactured In: United States
Units Affected: 13,800 tubes
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.