FDA recall D-0785-2022

Product

Pink Pussycat SENSUAL ENHANCEMENT capsule, 3000mg, 1-count blister card, Manufactured for: Pink Pussycat Products - Chatsworth, CA 91311, UPC 8 91875 00462 6.

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.

Distribution

Nationwide in the USA via walmart.com online marketplace

Key facts

Status

Terminated

Initiation date

2022-03-29

Report date

2022-04-27

Termination date

2024-07-31

Voluntary/Mandated

Voluntary: Firm initiated

Location

Chatsworth, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0785-2022