FDA Issues Recall on Enoki Mushrooms Amid Listeria Concerns

Enoki Mushroom 5.3 ozSubmitted Image

WASHINGTON, D.C. — The Food and Drug Administration (FDA) has announced a voluntary recall by Enoki King Mushroom Farm, based in Ventura, California, involving its 5.3-ounce packages of Enoki Mushrooms. This recall is due to potential contamination with Listeria monocytogenes, a serious pathogen posing significant health risks, particularly to vulnerable populations.

Listeria monocytogenes is known for causing severe and sometimes fatal infections, especially in young children, the elderly, and individuals with weakened immune systems. While healthy individuals might only experience temporary symptoms such as fever, headache, and gastrointestinal discomfort, the bacteria can lead to more serious complications, like miscarriages and stillbirths, in pregnant women.

The affected Enoki Mushrooms are packaged in clear plastic, labeled in both English and French. Consumers can identify these products by the lot code 4877 and UPC code 860011505600 printed on the packaging. These mushrooms were distributed through California and New York, reaching retail stores nationwide via produce distributors or wholesalers.

The recall was initiated following routine testing by the Maryland State Department of Health, which detected Listeria monocytogenes in a package of the product. As a precautionary measure, distribution has been halted to prevent further spread of potentially contaminated products.

To date, no illnesses have been reported in connection with this recall. However, the FDA urges consumers who have purchased these mushrooms with the specified lot code to return them to the place of purchase for a full refund. Consumers with questions or concerns can reach out to Enoki King Mushroom Farm directly at 718-290-6617, available Monday through Friday from 8 AM to 4 PM PST.

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