NRC Nutrition recalls Preconception Multi for Women 60-capsule blister packs (Batch 42469) due to inconsistent iodine blending. Consumers should check product labels for batch number.
inconsistent blending of iodine in the product
NRC Nutrition is recalling Preconception Multi for Women 60-capsule blister packs from Batch 42469 because iodine blending may be inconsistent. This could affect iodine levels in the supplement, though serious health risks are not specified in the recall.
The product contains inconsistent iodine blending, which could lead to uneven iodine levels in the supplement. Iodine is a critical nutrient for thyroid function and fetal development, but the recall does not specify if this inconsistency causes harm.
Women who purchased Preconception Multi for Women 60-capsule blister packs from Batch 42469. Those with iodine-sensitive health conditions may be at slightly higher risk.
Check for the batch number 42469 on the blister pack label. The product is sold as Preconception Multi for Women 60 capsules in blister packs.
Look for the batch number 42469 on the blister pack label to confirm if the product is affected.
The recall states inconsistent iodine blending but does not specify if this causes harm. NRC Nutrition has not stated that the product is unsafe for use.
The recall does not provide a remedy, so no action is required beyond checking the batch number.
The recall does not mention any risk of serious injury or death, so this is considered low risk.
We’ve drafted a message you can send NRC Nutrition to request your refund or repair — edit it as you like.
Subject: Recall F-0930-2025 — NRC Nutrition NRC Nutrition Hello, I own a NRC Nutrition that is covered by recall F-0930-2025 from NRC Nutrition. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
