Class IITerminatedVoluntary: Firm initiated
NRC Nutrition Pty Ltd: food recall F-0930-2025
NRC Nutrition Pty Ltd of Lytton recalled Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469. Reason: inconsistent blending of iodine in the product. The FDA listed it as Class II in its Enforcement Report dated Jun 18, 2025; distribution: California, Indiana, Minnesota, Oklahoma, Texas.
Record status as published: Terminated (terminated Jul 1, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469
- Product quantity
- 7 units
- Reason for recall
- inconsistent blending of iodine in the product
- Codes, lots and dates on the package
- Batch 42469
- Distribution pattern
- Texas, Minnesota, California, Indiana and Oklahoma
- Recalling firm
- NRC Nutrition Pty Ltd, Lytton, Australia
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Mar 29, 2025 |
| Classified by the FDA | Jun 9, 2025 |
| Published in the Enforcement Report | Jun 18, 2025 |
| Terminated | Jul 1, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0930-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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