SunGarden Mung Bean Sprouts 5lb & 10lb packaged in clear plastic bag in white cardboard box
Summary
The FDA issued a Class I for SunGarden Mung Bean Sprouts 5lb & 10lb packaged in clear plastic bag in whi by International Sprout Holding Inc.. Reason: Product tested positive for Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-0023-2022
Action Date
2021-10-27
Status
Terminated
Category
food
Product Description
SunGarden Mung Bean Sprouts 5lb & 10lb packaged in clear plastic bag in white cardboard box
Lot/Code Info: Lot Numbers: 251, 257, 264 Product Numbers: 122F, 124F Best By range 09/30/2021 to 10/13/2021
Quantity Affected: 360 cases total
Reason for Recall
Product tested positive for Listeria monocytogenes
Distribution
Distributed to a single customer in Florida
Type: Voluntary: Firm initiated
Recall Initiated: 2021-10-06
Company
Cookeville, TN
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 58 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (International Sprout Holding Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does International Sprout Holding Inc. have FDA actions?
This is the only FDA action we have on record for International Sprout Holding Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0023-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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