Food Recall Check
Class III · Low risk Ongoing Initiated Oct 29, 2025 (11 months ago)

Prenate Chewable¿ A chewable Rx prenatal vitamin with a delicious… recall

Recalled by Avion Pharmaceuticals, LLC · Alpharetta, GA, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

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.

Undeclared allergen: Soy

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Prenate Chewable¿ A chewable Rx prenatal vitamin with a delicious chocolate flavor with Quatrefolic Dietary Supplement 30 Tablets Rx Only UPC 3 75854 30630 2 Manufactured for: Avion Pharmaceuticals, LLC Alpharetta, GA 30005

Quantity: 804 bottles

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Product Code 75854-306-30 Lot 2402036 Exp 2026-04 Lot 2402036A Exp 2026-04 & Lot 2412020 Exp 2027-02

Where it was sold

Alabama Arizona California Colorado Florida Georgia Iowa Illinois Kentucky Massachusetts Missouri New York Ohio Oklahoma Pennsylvania Texas Virginia

FDA's distribution note: Product was shipped to the following states: AL, AZ, CA, CO, FL, GA, IA, IL, KY, MA, MO, NY, OH, OK, PA, TX & VA.

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. The risk from an undeclared allergen is to people allergic to soy; for anyone else the product is generally not a safety concern.

Recalling firm
Avion Pharmaceuticals, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 29, 2025
In FDA report of
Dec 10, 2025
FDA recall number
H-0233-2026 · event 97893
Official record
FDA enforcement report search