RecallHawk
Class I Recall

1. Welby Vitamin B12 Adult Gummies 140 Count 2. Berkely Jensen¿ Vitamin B12 1000 mcg Gummies 250 count 3. VitaGlobe" Vit

Vita Warehouse Corp.

Summary

The FDA issued a Class I for 1. Welby Vitamin B12 Adult Gummies 140 Count 2. Berkely Jensen¿ Vitamin B12 1000 by Vita Warehouse Corp.. Reason: Contains undeclared peanut.

Details

Source

Food Recall

External ID

H-0212-2025

Action Date

2025-07-09

Status

Terminated

Category

food

Product Description

1. Welby Vitamin B12 Adult Gummies 140 Count 2. Berkely Jensen¿ Vitamin B12 1000 mcg Gummies 250 count 3. VitaGlobe" Vitamin B12 Extra Strength Gummies 140 count 3. Vita Labs Vitamin B-12 Gummies Bulk 500 count

Lot/Code Info: 1. UPC Code: 4099100290868 Lot #: 248046601 Expiration Date: 10/2026 2. UPC Code: 888670132487 Lot #: 248046601 Expiration Date: 10/2026 3. UPC Code: 850005214670 Lot #: 248046601 Expiration Date: 10/2026 4. Lot# 248046601 Expiration date: 10/2026

Quantity Affected: 40,522 bottles plus 582,000 individual gummies

Reason for Recall

Contains undeclared peanut

Distribution

Nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2025-06-11

Company

Vita Warehouse Corp.

Ronkonkoma, NY

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 154 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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 (Vita Warehouse Corp.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Vita Warehouse Corp. have FDA actions?

This is the only FDA action we have on record for Vita Warehouse Corp. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0212-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for food

Related Actions