hCG Body Shaper — Class II drug recall D-0677-2017
Terminated recall by Gary Wood, reported 2017-05-03, distributed nationwide. Marketed without an Approved NDA/ANDA; FDA analysis has found the product to be tainted with human chorionic g
| Recall number | D-0677-2017 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Gary Wood, Saint Peters, MO, United States |
| Recall initiated | 2017-03-28 |
| Classified | 2017-04-21 |
| Reported by FDA | 2017-05-03 |
| Terminated | 2019-05-08 |
| Distributed | Nationwide (US) |
| Reason classes | unapproved product |
Product
hCG Body Shaper, Highly Purified Human Chorionic Gonadotrophin 5000 IU, Colloidal Silver B12, Stabilizers/Excipients, Not For Medical Use, Must Be Refrigerated, Distributed by HCG Body Shaper, St. Peters, MO
Reason for recall
Marketed without an Approved NDA/ANDA; FDA analysis has found the product to be tainted with human chorionic gonadotropin, rendering it an unapproved drug
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-0677-2017. 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.