Preconception Multi (NRC Nutrition) – Iodine Inconsistency (2025)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469
Brand
NRC Nutrition Pty Ltd
Lot Codes / Batch Numbers
Batch 42469
Products Sold
Batch 42469
NRC Nutrition Pty Ltd is recalling Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469 due to inconsistent blending of iodine in the product. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
inconsistent blending of iodine in the product
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, IN, MN, OK, TX
Page updated: Jan 7, 2026