Pink Toyz recalls Pink Pussycat SENSUAL ENHANCEMENT capsules (3000mg) due to containing undeclared sildenafil, an unapproved drug ingredient. FDA analysis found the product lacks required FDA approval.
Marketed Without An Approved NDA/ANDA: FDA analysis found the product to contain undeclared sildenafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
Pink Toyz is recalling Pink Pussycat SENSUAL ENHANCEMENT capsules because they contain undeclared sildenafil, an ingredient that requires FDA approval for sexual enhancement products. This makes the product an unapproved drug that could pose health risks.
The product contains undeclared sildenafil, an ingredient approved for male sexual enhancement in the U.S. without proper FDA approval. This makes the product an unapproved drug that could cause health risks if taken without medical supervision.
Anyone who owns or uses Pink Pussycat SENSUAL ENHANCEMENT capsules. People most at risk are those who take the capsules without knowing they contain an unapproved drug ingredient.
Look for Pink Pussycat SENSUAL ENHANCEMENT capsules with 3000mg strength, 1-count blister card, manufactured by Pink Toyz in Chatsworth, CA. The lot number is 2009066 and expiration date is 09/2023.
Identify if your capsule has the lot number 2009066 and expiration date 09/2023.
The FDA analysis found the product contains undeclared sildenafil, an unapproved drug ingredient. It is not safe to use without proper FDA approval.
The recall record does not specify a remedy, so contact Pink Toyz directly for guidance.
The FDA found the product contains undeclared sildenafil, an ingredient that requires FDA approval for sexual enhancement products, making it an unapproved drug.
We’ve drafted a message you can send Pink Toyz to request your refund or repair — edit it as you like.
Subject: Recall D-0785-2022 — Pink Toyz Pink Toyz Hello, I own a Pink Toyz that is covered by recall D-0785-2022 from Pink Toyz. 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.
