Pink Pussycat SENSUAL ENHANCEMENT capsule recalled over undeclared sildenafil
- Recall date
- March 29, 2022
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Pink Toyz recalls Pink Pussycat SENSUAL ENHANCEMENT capsule, 3000mg, 1-count blister card, Manufactured for: Pink Pussycat Products - Cha…
- Recall number
- D-0785-2022
- FDA classification
- Class I
- Brand / firm
- Pink Toyz
- Sold / distributed
- Nationwide in the USA via walmart.com online marketplace
Why it was recalled
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.
Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.
What was recalled
Pink Pussycat SENSUAL ENHANCEMENT capsule, 3000mg, 1-count blister card, Manufactured for: Pink Pussycat Products - Chatsworth, CA 91311, UPC 8 91875 00462 6.
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