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Unrated Drug recall · FDA · Published February 15, 2021

Adam's Secret Extra Strength 3000: FDA-Approved Drug Missing

Adam's Secret Extra Strength 3000 840mg blister packs (UPC 609728) were recalled by FDA for containing unapproved drugs tadalafil and sildenafil without proper FDA approval.

🇺🇸 FDA recall #D-0311-2021DrugAdams.Secret.co ›
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Recalling firmAdams.Secret.co29-31 Industrial Ave · Fairview, NJ 07022-1625
✎ GovInfoNow plain-language explainer

Adam's Secret Extra Strength 3000 840mg blister packs were recalled because they contain unapproved drugs tadalafil and sildenafil without FDA approval. This means the product is not legally approved for sale and could pose health risks. Read more at govinfonow.com/recall/36512-adam-s-secret-extra-strength-3000-fda-approved-drug-missing.

Source Summary by GovInfoNow · govinfonow.com/recall/36512-adam-s-secret-extra-strength-3000-fda-approved-drug-missing · Updated October 4, 2026 · FDA enforcement record: FDA #D-0311-2021

Cite this page

“Adam's Secret Extra Strength 3000: FDA-Approved Drug Missing.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36512-adam-s-secret-extra-strength-3000-fda-approved-drug-missing. Based on FDA recall #D-0311-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0311-2021%22&limit=1).

The Food and Drug Administration announced on Feb. 15, 2021, that Adams.Secret.co is recalling Adam's Secret Extra Strength 3000 products because they were marketed without an approved New Drug Application or Abbreviated New Drug Application. FDA analysis found the presence of tadalafil and sildenafil in the products.

How to tell if you have it

  • Adam's Secret Extra Strength 3000, 840 mg, 10 count blister packs
  • Distributed by AS Inc.
  • Made in USA
  • UPC 6 09728 43452 6

The hazard

The products were marketed without an approved New Drug Application or Abbreviated New Drug Application. FDA analysis results obtained the presence of tadalafil and sildenafil.

Context

GovInfoNow's records show other recent recalls of similar products include StuffbyNainax MR 7 SUPER 700000 Capsules (2025-12-15), SUN PHARMACEUTICAL Xyvona 3mg Tablets Recall (2026-05-22), and Shoolin Pharma Chem Sildenafil Recall (2026-08-03).

How to tell if you have this one

Check for Adam's Secret Extra Strength 3000 840mg 10-count blister packs with UPC 609728. The product was distributed by AS Inc. and made in the USA.

  • Brand
    Adams.Secret.co
  • Product
    Adam's Secret Extra Strength 3000, 840 mg, 10 count blister packs, Distributed by AS Inc., Made in USA, UPC 6 09728
  • Category
    Drug
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class I
  • Status
    Terminated
  • Distribution
    Nationwide in the USA
Recall numberProduct, codes & lotsQuantity
D-0310-2021Adam's Secret Extra Strength 1500, 800 mg, 10 count blister packs, Distributed by KP Inc., Made in USA, UPC 6 09728 43462 5; All lots within expiry.218 boxes
D-0311-2021Adam's Secret Extra Strength 3000, 840 mg, 10 count blister packs, Distributed by AS Inc., Made in USA, UPC 6 09728 43452 6.; All lots within expiry.N/A
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for Adam's Secret Extra Strength 3000 840mg 10-count blister packs with UPC 609728.

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

Distributed nationwide.

Recall timeline

FDA terminated this recall 14 months after the firm started it.

1. Firm started the recall: Feb 15, 202112. FDA classified it Class I: Mar 19, 202123. Published in FDA’s Enforcement Report: Mar 31, 202134. FDA terminated the recall: Apr 20, 2022420212022
  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-0311-2021 (February 15, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0311-2021 to see it in context.
  • Plain-language summary written by qwen3:4b on October 4, 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