FDA recall record
Gluta Plus (Glutathione) 60 capsules/container. UPC: NA
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 April 23, 2026. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Gluta Plus (Glutathione) 60 capsules/container. UPC: NA
Reason
undeclared allergen ingredient 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.
Gluta Plus (Glutathione) 60 capsules/container. UPC: NA
Code information listed by FDA
Lot codes: 231101V; 231142V; 241773V; 243381V
Distribution and firm information
Recalling firm listed by FDA: New Spirit Naturals Inc.
Firm location listed by FDA: San Dimas, CA, United States
Distribution reported by FDA: Products are sold directly to consumers via firm's online website.
Product quantity listed by FDA: 83 units
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.