The Recall Desk
HighFDA (Food)·F-0930-2025·Announced 2025-06-18

Preconception Multi for Women dietary supplement recalled for inconsistent iodine blending

NRC Nutrition is recalling Preconception Multi for Women Batch 42469 due to inconsistent iodine blending. The affected product was distributed in Texas, Minnesota, California, Indiana, and Oklahoma.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The FDA classified this as Class II. No illnesses or injuries have been reported. The hazard—inconsistent iodine blending—presents a theoretical risk of nutritional inadequacy or excess without confirmed harm, meeting the rubric criterion for High severity: a risk-of-harm product where injury has not yet been reported.

Plain-English summary

NRC Nutrition Pty Ltd is recalling Preconception Multi for Women 60 capsules (Batch 42469) packaged in blister packs due to inconsistent blending of iodine in the product.

The affected product was distributed in Texas, Minnesota, California, Indiana, and Oklahoma. A total of 7 units are involved in this recall.

Inconsistent iodine blending could result in some capsules containing insufficient or excessive levels of iodine, which may not provide the intended nutritional benefit or could potentially cause adverse effects. Consumers who have purchased this product should stop use and contact the manufacturer or their healthcare provider with questions.

The recalled product

Product
Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469
Manufacturer
NRC Nutrition Pty Ltd
Category
Food — Dietary Supplement
Hazard
  • iodine-variance
  • manufacturing-defect

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Batch 42469

Distribution

Distribution scope not specified by the agency.

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