Loud Muscle Science recalls 10-count Euphoria Capsules (ASIN B08ZJX4V9J) due to undeclared tadalafil, an unapproved drug ingredient. Consumers should stop using these capsules immediately.
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 10-count Euphoria Capsules because they contain undeclared tadalafil, an ingredient approved for male sexual enhancement. This makes the product an unapproved drug that could pose health risks.
The capsules contain undeclared tadalafil, a substance approved for male sexual enhancement treatments. Since this is an unapproved drug, it could cause health risks when taken without proper medical supervision.
Anyone who owns or uses these capsules is affected. People who have taken the capsules or plan to take them are at risk of health issues due to the unapproved drug ingredient.
Check for the 10-count tins with ASIN B08ZJX4V9J and UPC 661020846864. The lot number is 2022104 and expiration date is 04/2025.
Immediately stop using the recalled Euphoria Capsules as they contain an unapproved drug ingredient.
The capsules contain undeclared tadalafil, an ingredient approved for male sexual enhancement treatments, making them an unapproved drug.
Stop using them immediately and contact Loud Muscle Science for further instructions.
Yes, the capsules contain an unapproved drug ingredient that could pose health risks without proper medical supervision.
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-1337-2022 — Loud Muscle Science Loud Muscle Science Hello, I own a Loud Muscle Science that is covered by recall D-1337-2022 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.
