Junp Hydration recalls MegMan Performance Booster capsules due to undeclared tadalafil, an unapproved drug ingredient. This product was marketed without FDA approval and poses health risks.
Marketed Without An Approved NDA/ANDA: product was found to contain undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
Junp Hydration is recalling MegMan Performance Booster 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 product contains undeclared tadalafil, a substance approved for male sexual enhancement treatments. This makes it an unapproved drug that could cause health issues if used without proper medical supervision.
People who own or use MegMan Performance Booster capsules are affected. Those with underlying health conditions or who take medications may be at higher risk.
Check for MegMan Performance Booster capsules in 10-count blister packs with UPC 8 48998 00091 2. The product was sold with lot number 2010291 and expires January 7, 2024.
Look for MegMan Performance Booster capsules in 10-count blister packs with UPC 8 48998 00091 2.
The product contains undeclared tadalafil, an unapproved drug ingredient, so it is not safe to use without medical supervision.
The recall record does not specify a remedy, so contact Junp Hydration directly for guidance.
Check for MegMan Performance Booster capsules in 10-count blister packs with UPC 8 48998 00091 2, lot number 2010291, and expiration date January 7, 2024.
We’ve drafted a message you can send Junp Hydration to request your refund or repair — edit it as you like.
Subject: Recall D-0557-2022 — Junp Hydration Junp Hydration Hello, I own a Junp Hydration that is covered by recall D-0557-2022 from Junp Hydration. 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.
