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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
Medications & Supplements/Dietary Supplements

NRC Nutrition Preconception Multi for Women Recalled for Inconsistent Iodine

Agency Publication Date: June 9, 2025
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Summary

NRC Nutrition Pty Ltd is recalling 7 units of its Preconception Multi for Women dietary supplements (60 capsules packaged in blister packs) because of inconsistent iodine blending. Because the iodine was not mixed evenly, individual capsules may contain incorrect amounts of this mineral. No illnesses or injuries have been reported to date in connection with this issue.

Risk

Inconsistent levels of iodine in a supplement can lead to consumers receiving too much or too little of the nutrient, which may affect thyroid health or nutritional support during preconception.

What You Should Do

  1. The recalled products are Preconception Multi for Women (60 capsules) sold in blister packs labeled with Batch 42469 and Lot 42469.
  2. Return the product to the place of purchase for a full refund, throw it away, or contact NRC Nutrition Pty Ltd for further instructions.
  3. If you have additional questions, call the FDA Consumer Complaint hotline at 1-888-723-3332.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 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
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Preconception Multi for Women (60 capsules)by NRC Nutrition
Variants: Blister packs
Lot Numbers:
42469

Recall #: F-0930-2025; Batch 42469

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96811
Status: Resolved
Manufacturer: NRC Nutrition Pty Ltd
Sold By: specialty retailers
Manufactured In: Australia
Units Affected: 7 units
Distributed To: Texas, Minnesota, California, Indiana, Oklahoma

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 ยท 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.