# FDA recall D-1092-2017

> **Genetic Edge Compounds LLC** · Class I · drug recall initiated 2017-05-05.

## Product

GEC LX Laxoplex 60 capsules Dietary Supplement, 60 count bottle, Manufactured by GEC, McKinney, TX, 75070, UPC: 700580499842

## Reason for recall

Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplement: FDA analysis found the product to tainted with undeclared anabolic steroids and steroid like substances.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1092-2017
- **Recalling firm:** Genetic Edge Compounds LLC
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-05-05
- **Report date:** 2017-08-23
- **Termination date:** 2018-04-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** McKinney, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1092-2017

## Citation

> AI Analytics. FDA recall D-1092-2017. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-1092-2017. Source: US FDA. Licensed CC0.

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