Sung Soy Bean Sprouts, 1lb packages, in plastic packages, 20 bags per case
Summary
The FDA issued a Class I for Sung Soy Bean Sprouts, 1lb packages, in plastic packages, 20 bags per case by Samsung Bean Sprout. Reason: The firm initiated a recall of SoyBean Sprouts because product tested positive for Listeria monocytogenes..
Details
Source
Food Recall
External ID
F-0690-2024
Action Date
2024-01-10
Status
Terminated
Category
food
Product Description
Sung Soy Bean Sprouts, 1lb packages, in plastic packages, 20 bags per case
Lot/Code Info: Sell by date 12/14/23
Quantity Affected: 500 Bags
Reason for Recall
The firm initiated a recall of SoyBean Sprouts because product tested positive for Listeria monocytogenes.
Distribution
All products distributed to VA
Type: Voluntary: Firm initiated
Recall Initiated: 2023-12-20
Company
Jessup, MD
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 12 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Samsung Bean Sprout has 2 FDA actions in our database, including 2 recalls.
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 (Samsung Bean Sprout) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Samsung Bean Sprout have FDA actions?
Samsung Bean Sprout has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0690-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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