Severity
Moderate
ModerateClass IICompleted
FDA Food recall · Reported June 18, 2025
Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469
inconsistent blending of iodine in the product
Nrc Nutrition Pty Ltd recalled Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469 - a moderate-severity action.
Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469 was recalled by Nrc Nutrition Pty Ltd in June 18, 2025. Reason: inconsistent blending of iodine in the product. Check the official notice for the remedy. Verify recall #F-0930-2025 with the FDA Food before acting.
The recall
Nrc Nutrition Pty Ltd issued this moderate-severity FDA Food recall-inconsistent blending of iodine in the product.
- Moderate
- severity level
- 7 units
- affected scope
- Class II
- classification
- June 18, 2025
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0930-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0930-2025) was formally reported on June 18, 2025, with the manufacturer initiating the action on March 29, 2025. It is classified under Moderate severity (Class II), with a current status of Completed. Nrc Nutrition Pty Ltd is listed as the recalling firm, operating out of Lytton. Federal records list the affected scope as 7 units.
The documented reason for this recall is: inconsistent blending of iodine in the product Distribution data in the federal record shows the product reached: Texas, Minnesota, California, Indiana and Oklahoma. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Food recalls over time
Where this recall sits in its category - 25,126 food recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
7 units
Related Recalls
6
2 from same agency
Product description
Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469
Reason for recall
inconsistent blending of iodine in the product
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Completed |
| Recall number | F-0930-2025 |
| Date reported | June 18, 2025 |
| Date initiated | March 29, 2025 |
| Recalling firm | Nrc Nutrition Pty Ltd |
| Firm location | Lytton |
| Affected scope | 7 units |
| Distribution | Texas, Minnesota, California, Indiana and Oklahoma |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-0930-2025) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469. Recalled by Nrc Nutrition Pty Ltd. Units affected: 7 units.
Why was this product recalled? ▼
inconsistent blending of iodine in the product
Which agency issued this recall? ▼
This recall was issued by the FDA Food on June 18, 2025. Severity: Moderate. Recall number: F-0930-2025.
Where was the recalled product distributed? ▼
Distribution: Texas, Minnesota, California, Indiana and Oklahoma.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0930-2025) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported June 18, 2025. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.