RecallHawk
Class II 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

Nordic Naturals, Inc.

Summary

The FDA issued a Class II for Nordic Naturals Baby s Vitamin D3 liquid, 400 IU (10 mcg) D3, 0.76 fl oz (22.5 m by Nordic Naturals, Inc.. Reason: Elevated levels of vitamin D3.

Details

Source

Food Recall

External ID

F-1109-2024

Action Date

2024-04-03

Status

Terminated

Category

food

Product Description

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

Lot/Code Info: Lot number 234909

Quantity Affected: 5564 bottles

Reason for Recall

Elevated levels of vitamin D3

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.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-02-07

Company

Nordic Naturals, Inc.

Watsonville, CA

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 40 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Nordic Naturals, Inc. has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Nordic Naturals, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Nordic Naturals, Inc. have FDA actions?

Nordic Naturals, Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1109-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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