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Stop using now Drug recall · FDA · Published January 8, 2019

Happy Together Recalls 5K Premium Enhancement Capsules for Undeclared Drugs

FDA recalls Happy Together's 5K Premium Enhancement capsules due to undeclared sildenafil and tadalafil. Check your bottle if bought online.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-0388-2019DrugHappy Together ›
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Contact the company

Recalling firmHappy Together, Inc.1060 Audace Ave Apt 106 · Boynton Beach, FL 33426-3346
✎ GovInfoNow plain-language explainer

Happy Together, Inc. is recalling its 5K Premium Enhancement capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA). FDA analysis found the product was tainted with undeclared sildenafil and tadalafil, which are prescription ingredients not listed on the label. This poses a risk of unexpected side effects or interactions for consumers who do not know these drugs are present. Read more at govinfonow.com/recall/39252-happy-together-recalls-5k-premium-enhancement-capsules-for-undeclared-drugs.

Source Summary by GovInfoNow · govinfonow.com/recall/39252-happy-together-recalls-5k-premium-enhancement-capsules-for-undeclared-drugs · Updated October 11, 2026 · FDA enforcement record: FDA #D-0388-2019

Cite this page

“Happy Together Recalls 5K Premium Enhancement Capsules for Undeclared Drugs.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/39252-happy-together-recalls-5k-premium-enhancement-capsules-for-undeclared-drugs. Based on FDA recall #D-0388-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0388-2019%22&limit=1).

The Food and Drug Administration announced on Jan. 8, 2019, that Happy Together, Inc. recalled its 5K Premium Enhancement capsules because they were tainted with undeclared sildenafil and tadalafil. The FDA said the product was marketed without an approved New Drug Application or Abbreviated New Drug Application.

How to tell if you have it

  • Brand: Happy Together
  • Product: 5K Premium Enhancement Capsule, 5000 mg, 1 count blister card, box of 30
  • Company: Happy Together Inc., Boynton, FL
  • UPC: 00649964965644
  • Distribution: Sold over the internet

The hazard

The FDA said the product contained undeclared sildenafil and tadalafil. The agency classified the recall as Class I.

Context

GovInfoNow's records show other recent recalls of similar products include StuffbyNainax MR 7 SUPER 700000 Capsules (2025-12-15), Shoolin Pharma Chem Sildenafil Recall (2026-08-03), and Buy-Herbal Kian Pee Wan Capsules Recall (2026-03-21).

How to tell if you have this one

Look for a box containing 30 capsules in a 1-count blister card from Happy Together, Inc., located in Boynton, FL. The UPC is 649964965644. All lots within the expiry date are included in this recall.

  • Brand
    Happy Together
  • Product
    5K Premium Enhancement capsule, 5000 mg, 1 count blister card, box of 30, Happy Together Inc., Boynton, FL UPC
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Stop taking the capsules

    Do not consume any more of the product due to the presence of undeclared prescription drugs.

  2. Discard or return the product

    The recall record does not specify a specific remedy such as a refund or return address, so you should dispose of it safely or contact the seller for instructions.

How this recall unfolded

Recall timeline

FDA terminated this recall 2.8 years after the firm started it.

1. Firm started the recall: Jan 8, 201912. FDA classified it Class I: Jan 22, 201923. Published in FDA’s Enforcement Report: Jan 30, 201934. FDA terminated the recall: Oct 26, 2021420192021
  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-0388-2019 (January 8, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0388-2019 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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