FDA recall record

Hong Bin Foods Enoki Mushroom recall — FDA F-0890-2020

State of Michigan sampled and tested Enoki Mushrooms and found them to be positive for Listeria monocytogenes.

Class Iclassification
F-0890-2020official record ID
Apr 1, 2020report date

Recall record at a glance

Official recordF-0890-2020
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmHong Bin Foods LLC
Report dateApr 1, 2020
Recall initiation dateMar 6, 2020
QuantityUnknown
LocationMontebello, CA, United States

Official product description

Enoki Mushroom; Product of Korea; Net Wt. 7.05 oz., (200 g) UPC: 7 426852 625810 The Enoki is packaged in a clear film, bottom portion will be a green back group. With Enoki Mushroom in Orange letters, under that will be Product of Korea, 7.05 oz / 200g Sun Hong Foods, Inc. 1105 W. Oylmpic Blvd. Montebello, CA 90604 Codes on outside of box: This is what the Korea Broker H&P told us Outside the Box - PRODUCT OF KOREA Exporter Year Item Area Grower 01 10 09 153 100 Code 01 - Organization for Mushroom Association 01 means K-Mush Code 10 - Some kind of ID number form Mushroom Association. Code 09 - The Product and it is Enoki Mushroom Code 153 - Location of production: Qingbei District Code 100 - Specific Factory Number

Why the product was recalled

State of Michigan sampled and tested Enoki Mushrooms and found them to be positive for Listeria monocytogenes.

Distribution information

CA, TX, OR, WA, IL, FL

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: Telephone.

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

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