Enoki Mushroom Recall Due to Listeria monocytogenes Contamination
GREEN DAY PRODUCE is recalling enoki mushrooms (UPC 16430-69080) due to Listeria monocytogenes contamination. Affected products were distributed to retailers and distributors in 12 states.
The agency’s classification
FDA (Food): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: FDA Class I classification with confirmed Listeria monocytogenes contamination. Although no illnesses or deaths are reported, the agency's Class I designation and the high-risk pathogen require a Severe rating per the rubric.
Plain-English summary
GREEN DAY PRODUCE is recalling enoki mushrooms (200g per unit, UPC 16430-69080, product of Korea) because the product has been found to be contaminated with Listeria monocytogenes.
The recall affects 1,512 cases, with 25 units per case, that were distributed to 18 distributors and 10 retail locations in California, Minnesota, Utah, Arizona, Ohio, Florida, Illinois, Washington, Indiana, Michigan, Texas, and Georgia.
Consumers who have purchased this product should not consume it. Anyone with questions should contact GREEN DAY PRODUCE or the FDA.
This is an FDA Class I recall. The recall number is F-0183-2023.
The recalled product
- Product
- Enoki Mushroom Net wt. 200g (7.05 oz.) 25 units per case UPC: 16430-69080 Keep refrigerated Product of Korea
- Manufacturer
- GREEN DAY PRODUCE
- Category
- Food — Produce / Mushrooms
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- No code information on the product
Distribution
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