CLASS I Drug recall · Reported 27 Apr 2022 · FDA Enforcement Report
Pink Pussycat Sensual Enhancement capsule, 3000mg blister card recalled
Pink Toyz is recalling Pink Pussycat Sensual Enhancement capsule, 3000mg blister card, distributed nationwide in the US. The recall was initiated on 29 Mar 2022 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0785-2022
- FDA event ID
- 89949
- Recalling firm
- Pink Toyz, Chatsworth, CA
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 29 Mar 2022
- FDA classified
- 25 Apr 2022
- Reported
- 27 Apr 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Labeling Errors
Timeline
| 29 Mar 2022 | Recall initiated by company | |
| 25 Apr 2022 | Classified by FDA | +27 days |
| 27 Apr 2022 | Published in enforcement report | +2 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
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 as listed by the FDA
Pink Pussycat SENSUAL ENHANCEMENT capsule, 3000mg, 1-count blister card, Manufactured for: Pink Pussycat Products - Chatsworth, CA 91311, UPC 8 91875 00462 6.
Where it was distributed
Nationwide in the USA via walmart.com online marketplace
Stores named: Walmart
Questions about this recall
Why was it 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.
Which lots are affected?
Lot: 2009066, Exp: 09/2023
Where was it sold?
Nationwide in the USA via walmart.com online marketplace
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.