Enoki Mushrooms, brand Xuerong, net wt. 150 g/ 5.25200g/7.05-ounce packages, UPC 6953150110157. 34 0er carton.
Summary
The FDA issued a Class I for Enoki Mushrooms, brand Xuerong, net wt. 150 g/ 5.25200g/7.05-ounce packages, UPC by GOLDEN MEDAL MUSHROOM INC. Reason: Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-0813-2022
Action Date
2022-03-09
Status
Terminated
Category
food
Product Description
Enoki Mushrooms, brand Xuerong, net wt. 150 g/ 5.25200g/7.05-ounce packages, UPC 6953150110157. 34 0er carton.
Lot/Code Info: Lot 300511.
Quantity Affected: 88 cases
Reason for Recall
Listeria monocytogenes
Distribution
CA, TX, IL
Type: Voluntary: Firm initiated
Recall Initiated: 2022-02-23
Company
Commerce, CA
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 70 food recalls issued in the same week, part of 204 food-related FDA actions this month.
GOLDEN MEDAL MUSHROOM INC 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 (GOLDEN MEDAL MUSHROOM INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does GOLDEN MEDAL MUSHROOM INC have FDA actions?
GOLDEN MEDAL MUSHROOM INC 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-0813-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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