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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Drug
Medications & Supplements/Dietary Supplements

Launch Sequence Supplements Recalled for Undeclared Tadalafil

Agency Publication Date: August 12, 2022
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Summary

Loud Muscle Science is recalling several male enhancement products under the Launch Sequence brand, including standard capsules, Euphoria capsules, and Aphrodisia capsules. 12,416 units are affected because laboratory testing found they contain undeclared tadalafil, an FDA-approved ingredient used for male sexual enhancement, making these unapproved drugs. These supplements were sold nationwide in the USA and Canada, primarily through Amazon.com.

Risk

Tadalafil may interact with nitrates found in some prescription drugs, such as nitroglycerin, and may lower blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease frequently take nitrates, putting them at significant risk.

What You Should Do

  1. This recall affects Launch Sequence Capsules (60-count bottles), Euphoria Capsules (10-count tins), and Aphrodisia Capsules (4-count tins) sold under the Loud Muscle Science brand.
  2. Check your product packaging for UPC codes 641378938375, 661020846864, or 661020846957 and lot numbers including 20212001, 2022104, C07172101, or 2022054. See the Affected Products section below for the full list of affected codes.
  3. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) if you have further questions or wish to report an adverse event.

Your Remedy Options

You have 2 options:

💰Option 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
🗑️Option 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Launch Sequence Capsules, Dietary Supplement (60-count bottles)
Variants: 60-count bottles
UPC Codes:
641378938375
Lot Numbers:
20212001 (Exp 12/2024)
C07172101 (Exp 07/2024)
2022054 (Exp 03/2025)

ASIN B07TLPWXDS; Recall numbers D-1336-2022 and D-1339-2022.

Product: Launch Sequence Euphoria Capsules (10-count tins)
Variants: 10-count tins
UPC Codes:
661020846864
Lot Numbers:
2022104 (Exp 04/2025)
C07172101 (Exp 07/2024)

ASIN B08ZJX4V9J; Recall numbers D-1337-2022 and D-1340-2022.

Product: Launch Sequence Aphrodisia Capsules (4-count tins)
Variants: 4-count tins
UPC Codes:
661020846957
Lot Numbers:
2022104 (Exp 04/2025)
C07172101 (Exp 07/2024)

ASIN B07QB3S2LV; Recall numbers D-1338-2022 and D-1341-2022.

Product Images

“Loud Muscle, Launch Sequence, Men’s Health, 60 Capsules, dietary supplement”

“Loud Muscle, Launch Sequence, Men’s Health, 60 Capsules, dietary supplement”

“Loud Muscle, Launch Sequence, Aphrodisia”

“Loud Muscle, Launch Sequence, Aphrodisia”

“Loud Muscle, Launch Sequence, Euphoria”

“Loud Muscle, Launch Sequence, Euphoria”

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 90551
Status: Resolved
Manufacturer: Loud Muscle Science
Sold By: Amazon.com
Manufactured In: United States
Units Affected: 6 products (5,421 60-count bottles; 1000 10-count tins; 500 4-count tins; 2,495 60-count bottles; 1500 10-count tins; 1500 4-count tins)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · FDA Press Release · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.