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FDA recall record

Nordic Naturals Baby s Vitamin D3 liquid, 400 IU (10 mcg) D3, 0.76 fl oz (22.5 mL) DIETARY SUPPLEMENT, dark glass bottle

Recall F-1109-2024Class IITerminatedFebruary 7, 2024

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 June 21, 2024. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

Nordic Naturals Baby s Vitamin D3 liquid, 400 IU (10 mcg) D3, 0.76 fl oz (22.5 mL) DIETARY SUPPLEMENT, dark glass bottle

Reason

Elevated levels of vitamin D3

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.

  • Nordic Naturals Baby s Vitamin D3 liquid, 400 IU (10 mcg) D3, 0.76 fl oz (22.5 mL) DIETARY SUPPLEMENT, dark glass bottle

Code information listed by FDA

Lot number 234909

Distribution and firm information

Recalling firm listed by FDA: Nordic Naturals, Inc.

Firm location listed by FDA: Watsonville, CA, United States

Distribution reported by FDA: Products are distributed to 79 consignees, consisting of retailers, distributors, and consumers. Number of consignees who purchased through Amazon are unknown. U.S. distribution to AR, AZ, CA, DC, DE, FL, GA, IA, IL, IN, MA, MD, MI, MN, MO, MS, NC. ND, NH, NJ, NY, OH, OR, PA, RI, TX, VT and WI. Additionally, foreign customers in the Dubai and Kenya.

Product quantity listed by FDA: 5564 bottles

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.