Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469
Recalling firm: NRC Nutrition Pty Ltd
Why it was recalled
inconsistent blending of iodine in the product
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jul 1, 2026.
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ProductPreconception Multi for Women 60 capsules packaged in blister packs Batch 42469
FDA code information
Batch 42469
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Full FDA record and distribution details
Original product description
Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469
Original FDA recall reason
inconsistent blending of iodine in the product
Recall details
- Recall number
- F-0930-2025
- Event ID
- 96811
- FDA status
- Terminated
- Initiated
- Mar 29, 2025
- Reported
- Jun 18, 2025
- Classified
- Jun 9, 2025
- Terminated
- Jul 1, 2026
- Quantity
- 7 units
- Location
- Lytton, Australia
- Initiation type
- Voluntary: Firm initiated
- Notification
Where it was distributed
Texas, Minnesota, California, Indiana and Oklahoma
FDA source record · F-0930-2025
Data updated September 16, 2026. View official FDA data ↗
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