FDA recall record
RegenErect
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of August 8, 2017. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
RegenErect
Reason
The firm is recalling all herbal and dietary supplements because they were not manufactured in compliance with the current Good Manufacturing Practice regulations for Dietary Supplements.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
RegenErect
Code information listed by FDA
all lots
Distribution and firm information
Recalling firm listed by FDA: VivaCeuticals, Inc. dba Regeneca Worldwide
Firm location listed by FDA: Irvine, CA, United States
Distribution reported by FDA: US
Product quantity listed by FDA: unknown
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.