FDA recall record
FP0692, Confidence, Prenatal Multi-V + DHA, 90 tablets per bottle, UPC# 8 10891 02056 4
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 October 22, 2019. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
FP0692, Confidence, Prenatal Multi-V + DHA, 90 tablets per bottle, UPC# 8 10891 02056 4
Reason
Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol (PEG), Triacetin, FD&C Yellow #6 (Sunset Yellow FCF), FD&C Red #40 (Allura Red AC), FD&C Yellow #5 (Tartrazine), and FD&C Blue #2 (Indigotine).
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.
FP0692, Confidence, Prenatal Multi-V + DHA, 90 tablets per bottle, UPC# 8 10891 02056 4
Code information listed by FDA
Lot# 110516
Distribution and firm information
Recalling firm listed by FDA: Confidence Inc./Confidence U.S.A. Inc.
Firm location listed by FDA: Port Washington, NY, United States
Distribution reported by FDA: Nationwide
Product quantity listed by FDA: 5,650 bottles in US distribution (total for all products)
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.