Nordic Naturals Baby s Vitamin D3 liquid, 400 IU (10 mcg) D3, 0.76 fl oz (22.5 mL) DIETARY SUPPLEMENT, dark glass bottle — FDA record F-1109-2024

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Feb 7, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
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
Classification
Class II
Recalling firm
Nordic Naturals, Inc.
Quantity
5564 bottles
Agency-reported status
Terminated
Source record identifier
F-1109-2024

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityLot number 234909

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

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.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Apr 3, 2024
Recall initiation date
Feb 7, 2024
Center classification date
Mar 28, 2024
Termination date
Jun 21, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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