Recall: Progressive Laboratories, Xenesta Dietary Supplements
On 2018-02-23, the FDA announced that Progressive Laboratories is conducting a recall on Dietary Supplements due to possible undeclared milk. The recalled products were sold under the brand name(s) Progressive Laboratories and Xenesta during an unspecified time period throughout the regions shown in the map below.
In recent months, there have been 3 drugs recalls due to potential undeclared ingredients, including collagen protein dietary supplement, dietary supplement a1 slim and more. Additionally, there have been 18 drug and medical device recalls due to other health hazards as well as 73 food recalls.
Company Contact Information:
Name: Progressive Laboratories
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Detailed Recall Information
Regions Where Sold: Because the region was not specified, it is assumed that this product was available nationwide.
Product Description: Dietary supplements
Brand Name(s): Progressive Laboratories, Xenesta
Reason for Recall: Undeclared milk
Official Recall Date: 2018-02-23
Additional information provided by the FDA.gov:
Progressive Laboratories, Inc., located at 3131 Story Road West, Irving, Texas 75038, USA, is voluntarily recalling Testosterzone, Thyroid Resilience, Xenesta Nuvive Men's, and Xenesta Nuvive Women's, because it may contain an undeclared allergen. People who have an allergy or severe sensitivity to milk could run the risk of serious or life-threatening allergic reaction if they consume these products. 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.