Zhong Hua Jiu — Class II drug recall D-0624-2018
Terminated recall by United Pacific Co Ltd, reported 2018-04-18, distributed nationwide. CGMP Deviations: the product was produced with substandard GMP manufacturing processes.
| Recall number | D-0624-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | United Pacific Co Ltd, South El Monte, CA, United States |
| Recall initiated | 2018-03-29 |
| Classified | 2018-04-10 |
| Reported by FDA | 2018-04-18 |
| Terminated | 2019-01-24 |
| Distributed | Nationwide (US) |
| Quantity | 15,190 boxes |
| Reason classes | cgmp |
| NDC | 53614-0001-02 |
| Lot numbers | 12/30/20119, 14122921, 15091512, 17030921, 6032321 |
| Expiration dates | 2020-09-15, 2021-03-23, 2022-03-09 |
Product
Zhong Hua Jiu (menthol 1%) Patch, Distributed by United Pacific Company, UPC 6 924938 100226, NDC 53614-001-02
Reason for recall
CGMP Deviations: the product was produced with substandard GMP manufacturing processes.
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-0624-2018. 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.