Avion Pharmaceuticals recalls Prenate Chewable prenatal vitamins due to undeclared soy and incorrect boron labeling. Consumers should check product codes and contact the company for details.
Undeclared Soy. The firm received positive test results for soy which is not listed on the label. The firm also noticed that the amount of boron in the product is listed as 250mg per serving instead of 250mcg per serving.
Avion Pharmaceuticals is recalling Prenate Chewable prenatal vitamins because they contain undeclared soy and have a boron dosage error (250mg listed instead of 250mcg). This could lead to unintended soy exposure and boron intake risks for pregnant women.
The product contains soy that wasn't listed on the label, which could be a concern for people with soy allergies. Additionally, the boron content is listed as 250mg per serving instead of 250mcg, which is a significant error that could lead to excessive boron intake.
Pregnant women using the Prenate Chewable prenatal vitamins are most at risk due to potential soy exposure and boron dosage errors. The product is sold through pharmacies and online retailers.
Check for the UPC 3 75854 30630 2 on the product packaging. The product code is 75854-306-30 with lots 2402036 (expires 2026-04) and 2412020 (expires 2027-02).
Look for the UPC 3 75854 30630 2 or product code 75854-306-30 on the packaging.
The product has an undeclared soy ingredient and a boron dosage error, but the recall is for correction, not immediate danger. Consult the manufacturer for specific guidance.
Check the UPC 3 75854 30630 2 or product code 75854-306-30 with lots 2402036 (expires 2026-04) or 2412020 (expires 2027-02).
The recall does not specify a remedy, so contact Avion Pharmaceuticals directly for further instructions.
We’ve drafted a message you can send Avion Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall H-0233-2026 — Avion Pharmaceuticals Avion Pharmaceuticals Hello, I own a Avion Pharmaceuticals that is covered by recall H-0233-2026 from Avion Pharmaceuticals. 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.
