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GOLDEN MEDAL MUSHROOM INC Recall: Michigan Department of Agriculture and Rural Development sampled product and Listeria monocytogenes was detected.

United States

TerminatedClass I

Company
GOLDEN MEDAL MUSHROOM INC
Product
Enoki Mushrooms, brand Xuerong, net wt. 200g/7.05-ounce pack…
Recall date
February 4, 2022
Terminated
May 4, 2022
Source
FDA

Reason for recall

Michigan Department of Agriculture and Rural Development sampled product and Listeria monocytogenes was detected.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Enoki Mushrooms, brand Xuerong, net wt. 200g/7.05-ounce packages, UPC 6 953150 100684. Product sent to distributor is packaged in a brown cardboard master case. The product name "ENOKI MUSHROOM" and other information in Chinese are printed in green color. The code "300511" is printed in blue color. Not published in this source record 36 cartons lot # 300511

Distribution

  • Distributed in IL.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0738-2022
Event ID
89540
Status
Terminated
Classification
Class I
Company
GOLDEN MEDAL MUSHROOM INC
Product description
Enoki Mushrooms, brand Xuerong, net wt. 200g/7.05-ounce packages, UPC 6 953150 100684. Product sent to distributor is packaged in a brown cardboard master case. The product name "ENOKI MUSHROOM" and other information in Chinese are printed in green color. The code "300511" is printed in blue color.
Quantity
36 cartons
Reason
Michigan Department of Agriculture and Rural Development sampled product and Listeria monocytogenes was detected.
Recall initiation date
February 4, 2022
Report date
February 23, 2022
Classification date
Not published in this source record
Termination date
May 4, 2022
Distribution pattern
Distributed in IL.
UPC, lot, and code information
lot # 300511
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Press Release
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: GOLDEN MEDAL MUSHROOM INC

Other recalls from GOLDEN MEDAL MUSHROOM INC

FDA Recall United States Terminated Historical recordClass I

GOLDEN MEDAL MUSHROOM INC

Product
Enoki Mushrooms, brand Xuerong, net wt. 150 g/ 5.25200g/7.05…
Published
March 9, 2022
Distribution
Multiple states

View recall →

FDA Recall United States Terminated Historical recordClass I

GOLDEN MEDAL MUSHROOM INC

Product
Enoki Mushroom Product of Korea Net Wt. 200 g/7.05 oz. UPC:…
Published
May 5, 2021
Distribution
Nationwide

View recall →

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Illinois 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

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?

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