Food Recall Check
Class II · Moderate risk Completed Initiated Jun 13, 2025 (16 months ago)

vitamins B12 dietary supplement Raspberry Flavored sold under the following brand names recall

Recalled by Vitalabs, Inc. · McDonough, GA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Undeclared Peanuts. The firm was notified by their supplier, that the product may contain undeclared peanuts.

Undeclared allergen: Peanut

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

vitamins B12 dietary supplement Raspberry Flavored sold under the following brand names: 1. Black Girl Vitamins 60 gummies UPC 8 60008 57505 0 Manufactured for: Black Girl Vitamins 601 W Harrison St., Chicago, IL 60607. 2. Rise-N-Shine 17 Woodport Road, Sparta, NJ 07871 UPC 8 99130 01189 1

Quantity: 9,657 bottles

Food: Chocolate & candy Berries Dietary supplements

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.

1. LOT# 57221A BEST BY: 07/2026 and Lot# 56199 Best By: 07/2026 2. Lot# 57664 Best By: 07/2026

Where it was sold

Illinois New Jersey

FDA's distribution note: Product was shipped to IL & NJ.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to peanut; for anyone else the product is generally not a safety concern. FDA lists this recall as completed: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Vitalabs, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 13, 2025
In FDA report of
Oct 8, 2025
FDA recall number
H-0037-2026 · event 97084
Official record
FDA enforcement report search

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