FDA recall record
Xenesta Nuvive Womens 90 count packaged in a 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 Womens 90 count packaged in a 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 Womens 90 count packaged in a white plastic bottle with white cap
Code information listed by FDA
Lot # 2071957 and 2082387
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: 147 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.