Loud Muscle Science recalls 60-count Launch Sequence Capsules for containing undeclared tadalafil, an FDA-approved drug ingredient. This unapproved supplement poses health risks and requires immediate action.
Marketed Without An Approved NDA/ANDA: Product found to contain undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
Loud Muscle Science is recalling 60-count Launch Sequence Capsules because they contain undeclared tadalafil, an ingredient approved for male sexual enhancement. This makes the product an unapproved drug that could cause health risks.
The capsules contain undeclared tadalafil, a drug approved for male sexual enhancement. This makes the product an unapproved drug that could cause health risks like side effects from the active ingredient.
Anyone who owns or uses these capsules is affected. People with pre-existing health conditions or those taking other medications may be at higher risk.
Check for 60-count bottles labeled 'Launch Sequence Capsules' with ASIN B07TLPWXDS and UPC 641378938375. The lot number is 20212001 and expiration date is 12/2024.
Immediately stop using the recalled capsules as they contain an unapproved drug ingredient that could cause health risks.
The product contains undeclared tadalafil, an ingredient approved for male sexual enhancement, making it an unapproved drug.
Stop using it immediately and contact Loud Muscle Science for further instructions.
The product is an unapproved drug that could cause health risks, but the recall does not specify a risk of serious injury.
We’ve drafted a message you can send Loud Muscle Science to request your refund or repair — edit it as you like.
Subject: Recall D-1336-2022 — Loud Muscle Science Loud Muscle Science Hello, I own a Loud Muscle Science that is covered by recall D-1336-2022 from Loud Muscle Science. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
