Recall: Brian Richardson DBA "In Tha Pink" Ground Kopi Jantan Tradisional Natural Herbs Coffee
On 2019-04-05, the FDA announced that Brian Richardson DBA "In Tha Pink" is conducting a recall on Ground Kopi Jantan Tradisional Natural Herbs Coffee due to possible undeclared sildenafi, tadalafil. The recalled products were sold under the brand name(s) Brian Richardson DBA "In Tha Pink" during an unspecified time period throughout the regions shown in the map below.
In recent months, there have been 5 drugs recalls due to potential undeclared ingredients, including dietary supplement, detox capsules and more. Additionally, there have been 23 drug and medical device recalls due to other health hazards as well as 67 food recalls.
Company Contact Information:
Name: Brian Richardson DBA "In Tha Pink"
Phone: (214) 803-4652
Do you work for a company involved with this recall? Contact us to learn how you can control data, information and ads shown on this page.
Detailed Recall Information
Regions Where Sold: Because the region was not specified, it is assumed that this product was available nationwide.
Product Description: Ground Kopi Jantan Tradisional Natural Herbs Coffee
Brand Name(s): Brian Richardson DBA "In Tha Pink"
Reason for Recall: Undeclared Sildenafil and Tadalafil
Official Recall Date: 2019-04-05
Additional information provided by the FDA.gov:
Brian Richardson DBA "In Tha Pink", is voluntarily recalling lots with the expiration of October 13, 2020 (13/10/2020) of ground Kopi Jantan Tradisional Natural Herbs Coffee to the consumer level. FDA analysis has found the product to be tainted with Sildenafil and Tadalafil. Sildenafil and tadalafil are FDA approved drugs for the treatment of male erectile dysfunction. The presence of these undeclared active ingredients renders the product an unapproved drug for which safety and efficacy has not been established and, therefore, subject to recall. Read More.
More information may be available at FDA.gov
Latest Safety Recalls
Select image for details, including additional styles.
Sources may include Food & Drug Administration (FDA), United States Department of Agriculture (USDA), Health Canada and companies involved with this or a related recall.