Recall archive / FDA food enforcement
Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469 — FDA record F-0930-2025
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Mar 29, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469
- Reason
- inconsistent blending of iodine in the product
- Classification
- Class II
- Recalling firm
- NRC Nutrition Pty Ltd
- Quantity
- 7 units
- Agency-reported status
- Terminated
- Source record identifier
- F-0930-2025
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Batch 42469 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Texas, Minnesota, California, Indiana and Oklahoma
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Jun 18, 2025
- Recall initiation date
- Mar 29, 2025
- Center classification date
- Jun 9, 2025
- Termination date
- Jul 1, 2026
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.