RecallRadar
FDA · FoodClass I

Vita Warehouse Corp. food recall: 1. Welby Vitamin B12 Adult Gummies 140 Count 2. Berkely Jensen¿…

Undeclared allergens

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Terminated
Event ID
97062
Recall initiated
Jun 11, 2025
Classified by FDA
Jul 3, 2025
Posted in Enforcement Report
Jul 9, 2025
Terminated
Oct 28, 2025
Recalling firm
Vita Warehouse Corp.
Firm location
Ronkonkoma, NY, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Products in this event
1

What to do

Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.

View the official FDA record ↗

Reason for recall

Contains undeclared peanut

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Jun 11, 2025. FDA classified it 22 days later, on Jul 3, 2025. Distribution reported by FDA: Nationwide

Recalled products (1)

  • H-0212-2025 Class I Terminated

    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

    Codes / lots: 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: 40,522 bottles plus 582,000 individual gummies

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
Official notice
FDA Enforcement Report, event 97062
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.