Why it was recalled
inconsistent blending of iodine in the product
Product description
Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469
Lot numbers, UPCs & expiration codes
Batch 42469
Where it was sold
Texas, Minnesota, California, Indiana and Oklahoma
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- F-0930-2025
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Mar 29, 2025
- FDA report date
- Jun 18, 2025
- Quantity
- 7 units
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- NRC Nutrition Pty Ltd
Original FDA data
Every field from FDA enforcement report F-0930-2025, exactly as published.
Show all FDA fields
- City
- Lytton
- Status
- Terminated
- Country
- Australia
- Event ID
- 96811
- Address
- 12 Radar Street
- Code information
- Batch 42469
- Report date
- Jun 18, 2025
- Product type
- Food
- Recall number
- F-0930-2025
- Classification
- Class II
- Recalling firm
- NRC Nutrition Pty Ltd
- Product quantity
- 7 units
- Termination date
- Jul 1, 2026
- Reason for recall
- inconsistent blending of iodine in the product
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469
- Distribution pattern
- Texas, Minnesota, California, Indiana and Oklahoma
- Recall initiation date
- Mar 29, 2025
- Initial firm notification
- Center classification date
- Jun 9, 2025