On April 1, 2022, F&S Medical Supply, dba Pink Toyz, recalled one lot of Pink Pussycat 3000 mg capsules to the consumer level because FDA analysis found them to contain sildenafil.

Sildenafil (the active ingredient in Viagra) is prescribed for erectile dysfunction. This drug can cause symptoms like headache and flushing and can interact with medications containing nitrates such as nitroglycerine, resulting in dangerously low blood pressure.

Recalled Pink Pussycat 3000 mg products were sold by Pink Toyz and distributed nationwide through Walmart marketplaces. They are packaged in 1 count blister packs and can be identified by the following:

• UPC: 8 91875 00462 6
• LOT #: 2009066
• Expiration date of 09/2023

Consumers who purchased the recalled products should stop using them and return them to the place of purchase for a refund.

Consumers should also contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using these drug products. Consumers and healthcare providers can report any adverse reactions to the FDA's MedWatch Voluntary Reporting Program.

See ConsumerLab.com's Reviews of Sexual Enhancement Supplements for more information and tests of related products.

For more information, use the link below.

F&S Medical Supply, DBA Pink Toyz Issues Voluntary Nationwide Recall of Pink Pussycat Capsules Due to the Presence of Undeclared Sildenafil

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