Recall: 7K and Poseidon Dietary Supplements
On 2018-05-17, the FDA announced that Shoreside Enterprises is conducting a recall on Dietary Supplements due to possible undeclared sildenafil, tadalafil. The recalled products were sold under the brand name(s) 7K and Poseidon during an unspecified time period throughout the regions shown in the map below.
In recent months, there have been 8 drugs recalls due to potential undeclared ingredients, including "leanpro8" protein powder, marketed as dietary supplement- capsules and more. Additionally, there have been 22 drug and medical device recalls due to other health hazards as well as 94 food recalls.
Company Contact Information:
Name: Shoreside Enterprises
Phone: (727) 236-0576
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Detailed Recall Information
Regions Where Sold: Florida, Illinois, Massachusetts, North Carolina and Ohio
Product Description: Dietary Supplements
Brand Name(s): 7K and Poseidon
Reason for Recall: Undeclared Sildenafil and Tadalafil
Official Recall Date: 2018-05-17
Additional information provided by the FDA.gov:
Shoreside Enterprises, Inc. is voluntarily recalling 7K (Lot specific: Lot #RO) and Poseidon 4500 (Extreme 1000 mg) (Lot specific: Lot #20117BL) to the consumer level. FDA analysis found the samples of these products to contain undeclared Sildenafil and/or Tadalafil. Sildenafil and Tadalafil are active ingredients in two FDA-approved prescription drugs used for the treatment of erectile dysfunction (ED). The presence of Sildenafil and Tadalafil renders them unapproved drugs for which safety and efficacy have not been established and, therefore, subject to recall. Read More.
More information may be available at FDA.gov
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Sources may include Food & Drug Administration (FDA), United States Department of Agriculture (USDA), Health Canada and companies involved with this or a related recall.