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Home > Recalled Products > Drugs > Undetermined Hazard > ReGen Series Stem Cell Products

Recall: ReGen Series Stem Cell Products

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On 2018-10-10, the FDA announced that Liveyon is conducting a recall on Stem Cell Products due to a possible undetermined hazard. The recalled products were sold under the brand name(s) ReGen Series 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 undetermined hazard, including daptomycin for injection 500 mg, lyophilized powder for solution, single dose vial, birth control capsules and more. Additionally, there have been 28 drug and medical device recalls due to other health hazards as well as 67 food recalls.

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Company Contact Information:

Name: Liveyon
Website: www.liveyon.com
Phone: (800) 578-0983

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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: ReGen Series

Brand Name(s): ReGen Series

Reason for Recall: Adverse Reactions

Official Recall Date: 2018-10-10


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Additional information provided by the FDA.gov:

Liveyon, LLC ("Liveyon") is a distributor of stem cell products manufactured by Genetech, Inc. ("Genetech"), a laboratory located in San Diego, CA. Liveyon marketed and distributed these products under the trade name ReGen Series. Liveyon has voluntarily recalled all ReGen Series products due to reported possible adverse reactions. 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.

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