Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0930-2025.
inconsistent blending of iodine in the product
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0930-2025.
Recall ongoing. Follow firm instructions.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Nrc Nutrition Pty Ltd or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0930-2025.
NRC Nutrition Pty Ltd
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
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If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Nrc Nutrition Pty Ltd Recall FAQ
Nrc Nutrition Pty Ltd is the subject of a food safety report: Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469. The notice was published on March 29, 2025 by the U.S. Food and Drug Administration (FDA). Approximately 7 units are potentially affected.