FDA recall record

Marquis Worldwide Specialty Conah Organic Enoki Mushrooms recall — FDA F-0749-2021

California Department of Public Health sampled Conah Organic Enoki mushrooms with a positive result for Listeria monocytogenes.

Class Iclassification
F-0749-2021official record ID
Jul 7, 2021report date

Recall record at a glance

Official recordF-0749-2021
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmMarquis Worldwide Specialty Inc.
Report dateJul 7, 2021
Recall initiation dateMay 28, 2021
Quantity1,320 cases
LocationCity Of Industry, CA, United States

Official product description

Conah Organic Enoki Mushrooms; 200 g (7.05 oz.) clear package with orange bottom UPC 8 51511 00770 1 Distributed by: Marquis Worldwide Specialty Inc. City of Industry, CA 91748 Cook for a minimum of 7-8 mins before consumption.

Why the product was recalled

California Department of Public Health sampled Conah Organic Enoki mushrooms with a positive result for Listeria monocytogenes.

Distribution information

U.S. distribution to the following: CA, TX, and AZ. No foreign distribution.

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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.