FDA recall record
GNC, Womens Ultra Mega, Dietary Supplement, 180 Caplets,
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 July 27, 2017. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
GNC, Womens Ultra Mega, Dietary Supplement, 180 Caplets,
Reason
Undeclared Allergen: 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.
GNC, Womens Ultra Mega, Dietary Supplement, 180 Caplets,
Code information listed by FDA
GNC number: 202422, Nutra Manufacturing Lot Number: 3044FQ2024.
Distribution and firm information
Recalling firm listed by FDA: Nutra Manufacturing
Firm location listed by FDA: Greenville, SC, United States
Distribution reported by FDA: PA
Product quantity listed by FDA: 12,534 bottles/180 caplets per bottle.
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.