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Unrated Drug recall · FDA · Published May 19, 2017

Biotech Underground Tri-Ton Hardcore Formula capsules recalled: Unapproved steroids found

FDA found unapproved steroids in these dietary supplement capsules. Recalled due to potential health risks from unapproved substances. Consumers should check product details and contact manufacturer for guidance.

🇺🇸 FDA recall #D-1087-2017DrugDynamic Technical Formulations ›
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Recalling firmDYNAMIC TECHNICAL FORMULATIONS660 Hembree Pkwy Ste 115 · Roswell, GA 30076-4974
✎ GovInfoNow plain-language explainer

What happened, in plain English

Dynamic Technical Formulations recalled their Biotech Underground Tri: Tri-Ton Hardcore Formula capsules after FDA testing found unapproved steroids. This product was marketed as a dietary supplement but contains substances that require FDA approval for safety. Read more at govinfonow.com/recall/41605-biotech-underground-tri-ton-hardcore-formula-capsules-recalled-unapproved-steroids.

Source Summary by GovInfoNow · govinfonow.com/recall/41605-biotech-underground-tri-ton-hardcore-formula-capsules-recalled-unapproved-steroids · Updated October 8, 2026 · FDA enforcement record: FDA #D-1087-2017

Cite this page

“Biotech Underground Tri-Ton Hardcore Formula capsules recalled: Unapproved steroids found.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/41605-biotech-underground-tri-ton-hardcore-formula-capsules-recalled-unapproved-steroids. Based on FDA recall #D-1087-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1087-2017%22&limit=1).

Why it’s dangerous

The capsules were tested by the FDA and found to contain anarine and ostarine, which are unapproved substances. These substances are not approved for use in dietary supplements and could pose health risks if consumed.

Who’s affected

Anyone who owns or uses the 90-count Biotech Underground Tri-Ton Hardcore Formula capsules. People most at risk are those who have taken the product without knowing it contains unapproved steroids.

How to tell if you have this one

Check for the 90-count bottle labeled 'Biotech Underground Tri-Ton Hardcore Formula' distributed by Dynamic Technical Formulations. All lots of this product are affected.

  • Brand
    Dynamic Technical Formulations
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the 90-count bottle labeled 'Biotech Underground Tri-Ton Hardcore Formula' distributed by Dynamic Technical Formulations.

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: “U.S.A. 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 3 years after the firm started it.

1. Firm started the recall: May 19, 201712. FDA classified it Class I: Aug 14, 201723. Published in FDA’s Enforcement Report: Aug 23, 201734. FDA terminated the recall: May 7, 2020420172020
  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-1087-2017 (May 19, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1087-2017 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