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Samsung Bean Sprout Recall: Listeria monocytogenes.

United States

TerminatedClass I

Company
Samsung Bean Sprout
Product
Soy Bean Sprouts in a package labeled in part: Sam Sung Soy…
Recall date
December 29, 2023
Terminated
April 16, 2024
Source
FDA

Reason for recall

Listeria monocytogenes.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Soy Bean Sprouts in a package labeled in part: Sam Sung Soy Bean Sprouts, Net Wt. 1LB have a Sell By date of December 21, 2023. Not published in this source record 500 bags Sell By date of December 21, 2023

Distribution

  • The product was distributed in Virgnia .

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1114-2024
Event ID
93901
Status
Terminated
Classification
Class I
Company
Samsung Bean Sprout
Product description
Soy Bean Sprouts in a package labeled in part: Sam Sung Soy Bean Sprouts, Net Wt. 1LB have a Sell By date of December 21, 2023.
Quantity
500 bags
Reason
Listeria monocytogenes.
Recall initiation date
December 29, 2023
Report date
April 10, 2024
Classification date
Not published in this source record
Termination date
April 16, 2024
Distribution pattern
The product was distributed in Virgnia .
UPC, lot, and code information
Sell By date of December 21, 2023
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Samsung Bean Sprout

Other recalls from Samsung Bean Sprout

FDA Recall United States Terminated Historical recordClass I

Samsung Bean Sprout

Product
Sung Soy Bean Sprouts, 1lb packages, in plastic packages, 2…
Published
January 10, 2024
Distribution
All products distributed to VA

View recall →

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.