RecallRadar
FDA · FoodClass I

New Age International, Inc. food recall: Daily Veggies Enoki Mushroom

ListeriaMicrobial contamination

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Terminated
Event ID
96480
Recall initiated
Mar 11, 2025
Classified by FDA
Mar 19, 2025
Posted in Enforcement Report
Mar 26, 2025
Terminated
Aug 7, 2025
Recalling firm
New Age International, Inc.
Firm location
Brooklyn, 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

Contaminated with Listeria monocytogenes

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 Mar 11, 2025. FDA classified it 8 days later, on Mar 19, 2025. Distribution reported by FDA: Distributed to wholesalers in NY that distributed to other states. New Age International, Inc. has 3 recalls in our records.

Recalled products (1)

  • F-0646-2025 Class I Terminated

    Daily Veggies Enoki Mushroom; Product of Korea; Net WT. 200 g (7.05 oz); KEEP REFRIGERATED; Cook through before

    Codes / lots: UPC: 8809159458890

    Quantity: 2720 boxes

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 96480
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.

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