FDA Drug recall D-0785-2022
Pink Pussycat SENSUAL ENHANCEMENT capsule, 3000mg, 1-count blister card, Manufactured for: Pink Pussycat Products - Chatsworth, CA 91311, U…
- FDA Drug
- Class I
- terminated
- Published 2022-04-27
On 2022-04-27 the FDA classified a Class I recall of Pink Pussycat SENSUAL ENHANCEMENT capsule, 3000mg, 1-count blister card, Manufactured for: Pink Pussycat Products - Chatsworth, CA 91311, U… by Pink Toyz, citing 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 sexu….
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0785-2022 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2022-03-29 |
| Published | 2022-04-27 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Pink Toyz |
| Distribution | US |
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
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.
Identifiers
| upc | 891875004626 |
|---|---|
| code_info | Lot: 2009066, Exp: 09/2023 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0785-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.