FDA recall record
Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469
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 1, 2026. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469
Reason
inconsistent blending of iodine in the product
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.
Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469
Code information listed by FDA
Batch 42469
Distribution and firm information
Recalling firm listed by FDA: NRC Nutrition Pty Ltd
Firm location listed by FDA: Lytton, Australia
Distribution reported by FDA: Texas, Minnesota, California, Indiana and Oklahoma
Product quantity listed by FDA: 7 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.