Enoki Mushroom Net wt. 200g (7.05 oz.) 25 units per case UPC: 16430-69080 Keep refrigerated Product of Korea
Summary
The FDA issued a Class I for Enoki Mushroom Net wt. 200g (7.05 oz.) 25 units per case UPC: 16430-69080 Keep r by GREEN DAY PRODUCE. Reason: Product found to be contaminated with Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-0183-2023
Action Date
2022-12-14
Status
Terminated
Category
food
Product Description
Enoki Mushroom Net wt. 200g (7.05 oz.) 25 units per case UPC: 16430-69080 Keep refrigerated Product of Korea
Lot/Code Info: No code information on the product
Quantity Affected: 1512 cases, 25 units per case
Reason for Recall
Product found to be contaminated with Listeria monocytogenes
Distribution
Product was distributed to 18 distributors and 10 retail locations located in CA, MN, UT, AZ, OH, FL, IL, WA, IN, MI, TX, and GA.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-11-17
Company
Vernon, 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 16 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 (GREEN DAY PRODUCE) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does GREEN DAY PRODUCE have FDA actions?
This is the only FDA action we have on record for GREEN DAY PRODUCE in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0183-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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