Nordic Naturals Zero Sugar Kids Multivitamin Supplement - Gummies (120 gummies/bottle); 12 bottles/case
Summary
The FDA issued a Class III for Nordic Naturals Zero Sugar Kids Multivitamin Supplement - Gummies (120 gummies/b by Nordic Naturals, Inc.. Reason: Product is mislabeled..
Details
Source
Food Recall
External ID
F-0840-2025
Action Date
2025-06-11
Status
Terminated
Category
food
Product Description
Nordic Naturals Zero Sugar Kids Multivitamin Supplement - Gummies (120 gummies/bottle); 12 bottles/case
Lot/Code Info: Lot: 244423 RUS-30127 Expiration 05/2026
Quantity Affected: 1164 bottles (120 gummies/bottle)
Reason for Recall
Product is mislabeled.
Distribution
Domestic: AK, AZ, CA, CO, FL, GA, ID, IN, MA, MT, NC, ND, NH, NV, NY, OK, OR, RI, UT, WA; Foreign: Great Britain, UAE
Type: Voluntary: Firm initiated
Recall Initiated: 2025-05-02
Company
Watsonville, CA
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 123 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 III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
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-0840-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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