CLASS I Food recall · Reported 22 Jan 2025 · FDA Enforcement Report

Daily Veggies Enoki Mushroom recalled by New Age International

New Age International is recalling Daily Veggies Enoki Mushroom, distributed in Maryland, New York. The recall was initiated on 11 Dec 2024 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUPC code 8809159458890 on back label
Quantity recalled2177 boxes (25 units per box)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0398-2025
FDA event ID
95974
Recalling firm
New Age International, Brooklyn, NY
Classification
Class I
Status
Terminated
Recall initiated
11 Dec 2024
FDA classified
14 Jan 2025
Reported
22 Jan 2025
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Listeria
Product category
Fish

Timeline

11 Dec 2024Recall initiated by company
14 Jan 2025Classified by FDA+34 days
22 Jan 2025Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

may be contaminated with Listeria monocytogenes

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

Daily Veggies Enoki Mushroom, 200g Product of Korea UPC Codes: 8809159458890

Where it was distributed

NY, MD

MarylandNew York

Questions about this recall

Why was it recalled?

may be contaminated with Listeria monocytogenes

Which lots are affected?

UPC code 8809159458890 on back label

Where was it sold?

NY, MD

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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