Human Chorionic Gonadotropin 3000 IU — Class II drug recall D-0343-2019
Terminated recall by Pharm D Solutions, LLC, reported 2018-12-26, distributed in WA. Lack of Assurance of Sterility: Inadequate processes and equipment to assure the sterility of products intende
| Recall number | D-0343-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Pharm D Solutions, LLC, Houston, TX, United States |
| Recall initiated | 2018-11-19 |
| Classified | 2018-12-20 |
| Reported by FDA | 2018-12-26 |
| Terminated | 2020-10-13 |
| Distributed | WA |
| Quantity | 85 vials |
| Reason classes | sterility |
| NDC | 69699-1738-10 |
| Expiration dates | 2019-03-31 |
Product
Human Chorionic Gonadotropin 3000 IU, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054 1-844-263-6843 --- NDC: 69699-1738-10
Reason for recall
Lack of Assurance of Sterility: Inadequate processes and equipment to assure the sterility of products intended to be sterile.
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-0343-2019. 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.