# FDA recall D-0677-2017

> **Gary Wood** · Class II · drug recall initiated 2017-03-28.

## 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

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0677-2017
- **Recalling firm:** Gary Wood
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-03-28
- **Report date:** 2017-05-03
- **Termination date:** 2019-05-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Saint Peters, MO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0677-2017

## Citation

> AI Analytics. FDA recall D-0677-2017. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-0677-2017. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*