RecallHawk
Class II Recall

vitamins B12 dietary supplement Raspberry Flavored sold under the following brand names: 1. Black Girl Vitamins 60 gu

Vitalabs, Inc.

Summary

The FDA issued a Class II for vitamins B12 dietary supplement Raspberry Flavored sold under the following bran by Vitalabs, Inc.. Reason: Undeclared Peanuts. The firm was notified by their supplier, that the product may contain undeclared peanuts..

Details

Source

Food Recall

External ID

H-0037-2026

Action Date

2025-10-08

Status

Completed

Category

food

Product Description

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

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

Quantity Affected: 9,657 bottles

Reason for Recall

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

Distribution

Product was shipped to IL & NJ.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-06-13

Company

Vitalabs, Inc.

McDonough, GA

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 39 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Vitalabs, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Vitalabs, Inc. have FDA actions?

This is the only FDA action we have on record for Vitalabs, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0037-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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