FDA recall record

Jan Fruits Enoki Mushrooms 200g 50 units per box UPC: 851084 008358 Lot recall — FDA F-0420-2023

Product found to contain Listeria monocytogenes

Class Iclassification
F-0420-2023official record ID
Mar 22, 2023report date

Recall record at a glance

Official recordF-0420-2023
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmJan Fruits, Inc.
Report dateMar 22, 2023
Recall initiation dateFeb 24, 2023
Quantity310 cases
LocationVernon, CA, United States

Official product description

Enoki Mushrooms 200g 50 units per box UPC: 851084 008358 Lot #3779 on outside of box Imported from Taiwan Distributor: Jan Fruits, Inc. 426 Charter Way Vernon, CA 90058

Why the product was recalled

Product found to contain Listeria monocytogenes

Distribution information

Directly to California, then further distributed to Hawaii

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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