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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Food
Food & Beverages/Dietary Supplements

Nordic Naturals Baby's Vitamin D3 Recalled for Elevated Vitamin D3 Levels

Agency Publication Date: March 28, 2024
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Summary

Nordic Naturals, Inc. is recalling 5,564 bottles of Baby's Vitamin D3 liquid (400 IU) because the product contains elevated levels of vitamin D3 that exceed the amount listed on the label. The product was sold in 0.76 fluid ounce (22.5 mL) dark glass bottles through Amazon.com and other retailers. No illnesses or injuries have been reported to date, but the manufacturer initiated the recall after discovering the potency issue.

Risk

Taking excessive amounts of vitamin D3 can lead to vitamin D toxicity in infants. Symptoms may include nausea, vomiting, poor appetite, excessive thirst, and frequent urination, while severe cases can lead to serious health issues like kidney damage.

What You Should Do

  1. This recall affects Nordic Naturals Baby's Vitamin D3 liquid, 400 IU (10 mcg) D3, in 0.76 fl oz (22.5 mL) dark glass bottles with lot number 234909 and an expiration date of 12/25.
  2. Check the side of your bottle or the back of the outer packaging for the printed code 'Exp 12/25 Lot 234909' to determine if your supplement is part of this recall.
  3. Stop using the recalled product immediately.
  4. Return the product to the place of purchase for a full refund, throw it away, or contact Nordic Naturals for further instructions.
  5. If your child has consumed this product and is showing symptoms of vitamin D toxicity, contact your pediatrician or healthcare provider immediately.
  6. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional questions regarding this recall.

Your Remedy Options

You have 2 options:

💰Option 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
🗑️Option 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Nordic Naturals Baby's Vitamin D3 liquid (0.76 fl oz / 22.5 mL)
Variants: 400 IU (10 mcg) D3
UPC Codes:
768990027338
Lot Numbers:
234909 (Exp 12/25)

Packaged in dark glass bottles

Product Images

Nordic Nautrals Baby’s Vitamin D3 Liquid front panel bottle label

Nordic Nautrals Baby’s Vitamin D3 Liquid front panel bottle label

Nordic Nautrals Baby’s Vitamin D3 Liquid back panel bottle label, Exp 12/25 Lot 234909

Nordic Nautrals Baby’s Vitamin D3 Liquid back panel bottle label, Exp 12/25 Lot 234909

Nordic Nautrals Baby’s Vitamin D3 Liquid front panel box label

Nordic Nautrals Baby’s Vitamin D3 Liquid front panel box label

Nordic Nautrals Baby’s Vitamin D3 Liquid back panel box label, Exp 12/25 Lot 234909

Nordic Nautrals Baby’s Vitamin D3 Liquid back panel box label, Exp 12/25 Lot 234909

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93947
Status: Resolved
Manufacturer: Nordic Naturals, Inc.
Sold By: Amazon.com; retailers; distributors
Manufactured In: United States
Units Affected: 5564 bottles
Distributed To: 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

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · FDA Press Release · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.