Pink Toyz: Drug Recall
Recall #D-0785-2022 · 03/29/2022
Class I: Dangerous
Recall Details
- Recall Number
- D-0785-2022
- Classification
- Class I
- Product Type
- Drug
- Recalling Firm
- Pink Toyz
- Status
- Terminated
- Date Initiated
- 03/29/2022
- Location
- Chatsworth, CA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 120 blister cards
Reason for Recall
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.
Product Description
Pink Pussycat SENSUAL ENHANCEMENT capsule, 3000mg, 1-count blister card, Manufactured for: Pink Pussycat Products - Chatsworth, CA 91311, UPC 8 91875 00462 6.
Distribution Pattern
Nationwide in the USA via walmart.com online marketplace
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.