CLASS I Food recall · Reported 14 Dec 2022 · FDA Enforcement Report

Enoki Mushroom recalled by Green Day Produce

Green DAY Produce is recalling Enoki Mushroom, distributed in 12 states. The recall was initiated on 17 Nov 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesNo code information on the product
Quantity recalled1512 cases, 25 units per case

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-0183-2023
FDA event ID
91167
Recalling firm
Green DAY Produce, Vernon, CA
Brand
Enoki
Classification
Class I
Status
Terminated
Recall initiated
17 Nov 2022
FDA classified
2 Dec 2022
Reported
14 Dec 2022
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Listeria
Product category
Mushrooms

Timeline

17 Nov 2022Recall initiated by company
2 Dec 2022Classified by FDA+15 days
14 Dec 2022Published in enforcement report+12 days

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

Reason for recall

Product found to 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

Enoki Mushroom Net wt. 200g (7.05 oz.) 25 units per case UPC: 16430-69080 Keep refrigerated Product of Korea

Where it was distributed

Product was distributed to 18 distributors and 10 retail locations located in CA, MN, UT, AZ, OH, FL, IL, WA, IN, MI, TX, and GA.

ArizonaCaliforniaFloridaGeorgiaIllinoisIndianaMichiganMinnesotaOhioTexasUtahWashington

Questions about this recall

Why was it recalled?

Product found to be contaminated with Listeria monocytogenes

Which lots are affected?

No code information on the product

Where was it sold?

Product was distributed to 18 distributors and 10 retail locations located in CA, MN, UT, AZ, OH, FL, IL, WA, IN, MI, TX, and GA.

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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