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Stop using now Drug recall · FDA · Published May 5, 2017

Genetic Edge Laxoplex Capsules Recalled: Unapproved Steroids Found

FDA found undeclared anabolic steroids in Genetic Edge Laxoplex capsules. All 60-count bottles are recalled due to potential health risks from unapproved substances.

🇺🇸 FDA recall #D-1092-2017DrugGenetic Edge ›
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Recalling firmGenetic Edge Compounds LLC2305 Brandywine · McKinney, TX 75070-4563
✎ GovInfoNow plain-language explainer

What happened, in plain English

Genetic Edge's Laxoplex 60-capsule dietary supplement has been recalled because FDA testing found it contains undeclared anabolic steroids and steroid-like substances. This poses health risks as these substances are not approved for use in dietary supplements. Read more at govinfonow.com/recall/41633-genetic-edge-laxoplex-capsules-recalled-unapproved-steroids-found.

Source Summary by GovInfoNow · govinfonow.com/recall/41633-genetic-edge-laxoplex-capsules-recalled-unapproved-steroids-found · Updated October 8, 2026 · FDA enforcement record: FDA #D-1092-2017

Cite this page

“Genetic Edge Laxoplex Capsules Recalled: Unapproved Steroids Found.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/41633-genetic-edge-laxoplex-capsules-recalled-unapproved-steroids-found. Based on FDA recall #D-1092-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1092-2017%22&limit=1).

Why it’s dangerous

The product was marketed as a dietary supplement but contains undeclared anabolic steroids and steroid-like substances that are not approved by the FDA. These substances can cause health issues including hormonal imbalances and other serious health problems when taken without proper medical supervision.

Who’s affected

Anyone who owns or uses the recalled Laxoplex 60-capsule bottles. People taking the product for weight loss or muscle building are at highest risk due to potential health effects from unapproved substances.

How to tell if you have this one

Check for the 60-count bottle labeled 'GEC LX Laxoplex 60 capsules Dietary Supplement'. The product was manufactured by Genetic Edge Compounds LLC in McKinney, TX, and sold with the UPC 700580499842. All lots are affected.

  • Brand
    Genetic Edge
  • Product
    GEC LX Laxoplex 60 capsules Dietary Supplement, 60 count bottle, Manufactured by GEC, McKinney, TX, 75070, UPC
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Now

    Immediately stop using the recalled Laxoplex 60-capsule bottles as they contain undeclared anabolic steroids and steroid-like substances.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 11 months after the firm started it.

1. Firm started the recall: May 5, 201712. FDA classified it Class I: Aug 15, 201723. Published in FDA’s Enforcement Report: Aug 23, 201734. FDA terminated the recall: Apr 5, 2018420172018
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-1092-2017 (May 5, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1092-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 8, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA