Daily Veggies Enoki Mushroom; Product of Korea; Net WT. 200 g (7.05 oz); KEEP REFRIGERATED; Cook through before
Summary
The FDA issued a Class I for Daily Veggies Enoki Mushroom; Product of Korea; Net WT. 200 g (7.05 oz); KEEP RE by New Age International, Inc.. Reason: Contaminated with Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-0646-2025
Action Date
2025-03-26
Status
Terminated
Category
food
Product Description
Daily Veggies Enoki Mushroom; Product of Korea; Net WT. 200 g (7.05 oz); KEEP REFRIGERATED; Cook through before
Lot/Code Info: UPC: 8809159458890
Quantity Affected: 2720 boxes
Reason for Recall
Contaminated with Listeria monocytogenes
Distribution
Distributed to wholesalers in NY that distributed to other states.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-03-11
Company
Brooklyn, NY
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 53 food recalls issued in the same week, part of 204 food-related FDA actions this month.
New Age International, Inc. has 3 FDA actions in our database, including 3 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 (New Age International, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does New Age International, Inc. have FDA actions?
New Age International, Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0646-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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