CLASS II Food recall · Reported 18 Jun 2025 · FDA Enforcement Report
Preconception Multi for Women recalled by NRC Nutrition Pty
NRC Nutrition Pty is recalling Preconception Multi for Women, distributed in California, Indiana, Minnesota, Oklahoma, Texas. The recall was initiated on 29 Mar 2025 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0930-2025
- FDA event ID
- 96811
- Recalling firm
- NRC Nutrition Pty, Lytton
- Brand
- Preconception Multi
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 29 Mar 2025
- FDA classified
- 9 Jun 2025
- Reported
- 18 Jun 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Packaging Defects
- Product category
- Dietary Supplements
Timeline
| 29 Mar 2025 | Recall initiated by company | |
| 9 Jun 2025 | Classified by FDA | +72 days |
| 18 Jun 2025 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
inconsistent blending of iodine in the product
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469
Where it was distributed
Texas, Minnesota, California, Indiana and Oklahoma
Questions about this recall
Why was it recalled?
inconsistent blending of iodine in the product
Which lots are affected?
Batch 42469
Where was it sold?
Texas, Minnesota, California, Indiana and Oklahoma
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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