CLASS I Food recall · Reported 27 Oct 2021 · FDA Enforcement Report

SunGarden Mung Bean Sprouts recalled by International Sprout Holding

International Sprout Holding is recalling SunGarden Mung Bean Sprouts, distributed in Florida. The recall was initiated on 6 Oct 2021 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot Numbers: 251, 257, 264 Product Numbers: 122F, 124F Best By range 09/30/2021 to 10/13/2021
Quantity recalled360 cases total

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-0023-2022
FDA event ID
88834
Recalling firm
International Sprout Holding, Cookeville, TN
Classification
Class I
Status
Terminated
Recall initiated
6 Oct 2021
FDA classified
15 Oct 2021
Reported
27 Oct 2021
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Listeria
Product category
Sprouts

Timeline

6 Oct 2021Recall initiated by company
15 Oct 2021Classified by FDA+9 days
27 Oct 2021Published 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 tested positive for 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

SunGarden Mung Bean Sprouts 5lb & 10lb packaged in clear plastic bag in white cardboard box

Where it was distributed

Distributed to a single customer in Florida

Florida

Questions about this recall

Is SunGarden Mung Bean Sprouts recalled?

Yes. International Sprout Holding recalled SunGarden Mung Bean Sprouts on 6 Oct 2021. The recall is Class I and its status is Terminated. Recall number F-0023-2022.

Why was it recalled?

Product tested positive for Listeria monocytogenes

Which lots are affected?

Lot Numbers: 251, 257, 264 Product Numbers: 122F, 124F Best By range 09/30/2021 to 10/13/2021

Where was it sold?

Distributed to a single customer in Florida

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 21 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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