FDA Drug recall D-0031-2018
PIYANPING Anti-Itch (hydrocortisone) Lotion, 1%, Net Wt. 0.67 oz (20g) tube, Manufactured By: Jimin Pharmaceutial Co., LTD., Distributor: L…
- FDA Drug
- Class I
- terminated
- Published 2017-11-01
On 2017-11-01 the FDA classified a Class I recall of PIYANPING Anti-Itch (hydrocortisone) Lotion, 1%, Net Wt. 0.67 oz (20g) tube, Manufactured By: Jimin Pharmaceutial Co., LTD., Distributor: L… by Lucky Mart, citing incorrect Product Formulation: product contains dexamethasone instead of hydrocortisone.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0031-2018 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2017-08-29 |
| Published | 2017-11-01 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Lucky Mart |
| Distribution | US |
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
Incorrect Product Formulation: product contains dexamethasone instead of hydrocortisone.
Identifiers
| code_info | Lot #: C16001, C16002, Exp 12/18 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0031-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.