FindMyRecallSubscribe
Class I: serious health riskTerminated

Pink Pussycat SENSUAL ENHANCEMENT capsule Recall

Pink Pussycat SENSUAL ENHANCEMENT capsule, 3000mg, 1-count blister card, Manufactured f…

Pink Toyz · Chatsworth, CA

Risk level
Class I
Reported by FDA
Apr 27, 2022
Recall ID
D-0785-2022
Check your lot numberHow we source this data

Summary

Pink Toyz recalled Pink Pussycat SENSUAL ENHANCEMENT capsule starting Mar 29, 2022. The FDA classified it as Class I (serious health risk) and published enforcement report D-0785-2022 on Apr 27, 2022. 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. Status: Terminated.

Why it was 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.

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.

Lot numbers, UPCs & expiration codes

Lot: 2009066, Exp: 09/2023

Where it was sold

Nationwide in the USA via walmart.com online marketplace

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0785-2022
Classification
Class I
Status
Terminated
Recall initiated
Mar 29, 2022
FDA report date
Apr 27, 2022
Quantity
120 blister cards
Recall type
Voluntary: Firm initiated
Recalling firm
Pink Toyz

Original FDA data

Every field from FDA enforcement report D-0785-2022, exactly as published.

Show all FDA fields
City
Chatsworth
State
CA
Status
Terminated
Country
United States
Event ID
89949
Address
9180 Gazette Ave
Code information
Lot: 2009066, Exp: 09/2023
Postal code
91311-5917
Report date
Apr 27, 2022
Product type
Drugs
Recall number
D-0785-2022
Classification
Class I
Recalling firm
Pink Toyz
Product quantity
120 blister cards
Termination date
Jul 31, 2024
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.
Voluntary / mandated
Voluntary: Firm initiated
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
Recall initiation date
Mar 29, 2022
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Apr 25, 2022

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0785-2022, published Apr 27, 2022. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

How we source and update recall data · Report incorrect information

Other recent drug recalls