Food Recall Check
Class I · High risk Terminated Initiated Jun 11, 2025 (16 months ago)

1. Welby Vitamin B12 Adult Gummies recall

Recalled by Vita Warehouse Corp. · Ronkonkoma, NY, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Contains undeclared peanut

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

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

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

Food: Chocolate & candy

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. 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

Where it was sold

Nationwide.

FDA's distribution note: Nationwide

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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 terminated: 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
Vita Warehouse Corp.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 11, 2025
In FDA report of
Jul 9, 2025
Terminated
Oct 28, 2025
FDA recall number
H-0212-2025 · event 97062
Official record
FDA enforcement report search

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