PIYANPING Anti-Itch — Class I drug recall D-0031-2018
Terminated recall by Lucky Mart Inc., reported 2017-11-01, distributed nationwide. Incorrect Product Formulation: product contains dexamethasone instead of hydrocortisone.
| Recall number | D-0031-2018 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Lucky Mart Inc., South El Monte, CA, United States |
| Recall initiated | 2017-08-29 |
| Classified | 2017-10-24 |
| Reported by FDA | 2017-11-01 |
| Terminated | 2018-10-30 |
| Distributed | Nationwide (US) |
| Quantity | 13,800 tubes |
| NDC | 68085-8012-04 |
| Lot numbers | 0.67, 12/18, C16001, C16002 |
Product
PIYANPING Anti-Itch (hydrocortisone) Lotion, 1%, Net Wt. 0.67 oz (20g) tube, Manufactured By: Jimin Pharmaceutial Co., LTD., Distributor: Lucky Mart, El Monte, CA 91733, NDC 68085-8012-4.
Reason for recall
Incorrect Product Formulation: product contains dexamethasone instead of hydrocortisone.
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-0031-2018. 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.