FDA recall record
Xenesta Nuvive Mens 90 count packaged in an white plastic bottle with white cap
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 7, 2018. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Xenesta Nuvive Mens 90 count packaged in an white plastic bottle with white cap
Reason
Recalled dietary supplements may contain undeclared milk.
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.
Xenesta Nuvive Mens 90 count packaged in an white plastic bottle with white cap
Code information listed by FDA
Lot # 2071887
Distribution and firm information
Recalling firm listed by FDA: Progressive Laboratories, Inc
Firm location listed by FDA: Irving, TX, United States
Distribution reported by FDA: Nationwide through the United States
Product quantity listed by FDA: 88 boxes (2 bottles/box)
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.