FDA recall record

Fuji Food Products Okami brand 8pc Supreme California Roll, SKU 28103 recall — FDA F-0418-2020

RTE products potentially contaminated with Listeria monocytogenes.

Class Iclassification
F-0418-2020official record ID
Jan 1, 2020report date

Recall record at a glance

Official recordF-0418-2020
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmFuji Food Products, Inc.
Report dateJan 1, 2020
Recall initiation dateNov 26, 2019
QuantityTBD
LocationBrockton, MA, United States

Official product description

Okami brand 8pc Supreme California Roll, SKU 28103

Why the product was recalled

RTE products potentially contaminated with Listeria monocytogenes.

Distribution information

AL, DE, FL, GA, IL, IN, IA, KS,KY, ME, MD,MA,MI,MN,MS,MO, NE, NH,NJ, NY,NC,OH,PA, RI, SC,TN,VT,VA, WV,DC, WV,WI

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.

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