HCG — Class II drug recall D-1420-2014
Terminated recall by Brookfield Prescription Center Inc. dba MD Custom Rx, reported 2014-07-09, distributed in WI. Incorrect/Undeclared Excipients: Specific drug products were compounded with an incorrect solvent.
| Recall number | D-1420-2014 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Brookfield Prescription Center Inc. dba MD Custom Rx, Brookfield, WI, United States |
| Recall initiated | 2014-05-30 |
| Classified | 2014-07-03 |
| Reported by FDA | 2014-07-09 |
| Terminated | 2015-05-22 |
| Distributed | WI |
| Quantity | 55 ml |
| Reason classes | undeclared allergen |
| Expiration dates | 2014-06-15, 2014-06-22, 2014-06-24, 2014-07-08, 2014-07-12 |
Product
HCG (Human Chorionic Gonadotropin) 200 units/ 0.1 mL drops, packaged in 5 mL and 10 mL bottles, Rx only, MD Custom Rx, 19035 W. Capitol Dr., Ste. 105, Brookfield, WI 53045
Reason for recall
Incorrect/Undeclared Excipients: Specific drug products were compounded with an incorrect solvent.
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-1420-2014. 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.