Food Recall Check
Class II · Moderate risk Terminated Initiated Feb 7, 2024 (3 years ago)

Nordic Naturals Baby s Vitamin D3 liquid recall

Recalled by Nordic Naturals, Inc. · Watsonville, CA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Elevated levels of vitamin D3

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

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

Quantity: 5564 bottles

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot number 234909

Where it was sold

Arkansas Arizona California District of Columbia Delaware Florida Georgia Iowa Illinois Indiana Massachusetts Maryland Michigan Minnesota Missouri Mississippi North Carolina North Dakota New Hampshire New Jersey New York Ohio Oregon Pennsylvania Rhode Island Texas Vermont Wisconsin

FDA's distribution note: 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.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Nordic Naturals, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 7, 2024
In FDA report of
Apr 3, 2024
Terminated
Jun 21, 2024
FDA recall number
F-1109-2024 · event 93947
Official record
FDA enforcement report search

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