Recall: Regeneca Worldwide Various Herbal And Dietary Supplements
On 2017-03-09, the FDA announced that Regeneca Worldwide is conducting a recall on Various Herbal And Dietary Supplements due to a possible . The recalled products were sold under the brand name(s) Regeneca Worldwide during an unspecified time period throughout the regions shown in the map below.
In recent months, there have been 2 drugs recalls due to potential unintended use, including non-sterile drug products, male sex enhancer dietary supplement and more. Additionally, there have been 11 drug and medical device recalls due to other health hazards as well as 131 food recalls.
Company Contact Information:
Name: Regeneca Worldwide
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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: Various herbal and dietary supplements
Brand Name(s): Regeneca Worldwide
Reason for Recall: Not manufactured in compliance with cGMPs
Official Recall Date: 2017-03-09
Additional information provided by the FDA.gov:
Regeneca Worldwide, a division of VivaCeuticals, Inc. is conducting a nationwide recall of its entire line of herbal and dietary supplement products pursuant to a Consent Decree entered by the federal court for the Central District of California. This recall applies to all products manufactured and sold between June 1, 2011 and February 8, 2017. 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.