# FDA recall D-0785-2022

> **Pink Toyz** · Class I · drug recall initiated 2022-03-29.

## 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

- **Recall number:** D-0785-2022
- **Recalling firm:** Pink Toyz
- **Classification:** Class I
- **Product type:** drug
- **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

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

## Citation

> AI Analytics. FDA recall D-0785-2022. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0785-2022. Source: US FDA. Licensed CC0.

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