FDA Recalls Okami Spicy Supreme California Rolls for Listeria Risk
Fuji Food Products is recalling Okami brand 8pc Spicy Supreme California Rolls due to potential Listeria monocytogenes contamination.
What this means for you
Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.
Our severity reasoning: The source text explicitly identifies the agency classification as Class I, which mandates a severity score of 5 according to the rubric.
Plain-English summary
The U.S. Food and Drug Administration has issued a Class I recall for Okami brand 8pc Spicy Supreme California Rolls, SKU 28104. The product is being recalled because it is a ready-to-eat (RTE) item potentially contaminated with Listeria monocytogenes.
The recall involves 75,821 units of the product. The affected items have date codes ranging from 11/22/2019 to 12/06/2019. The product was distributed in the following states and districts: 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, and WI.
Consumers who have purchased this product should stop eating it immediately. Listeria monocytogenes can cause serious illness, particularly in pregnant women, newborns, the elderly, and individuals with weakened immune systems. Consumers should check their pantries for the specific SKU and date code range listed above and discard the product or return it to the place of purchase.
The recalled product
- Product
- Okami brand 8pc Spicy Supreme California Roll, SKU 28104
- Manufacturer
- Fuji Food Products, Inc.
- Category
- Food — Ready-to-Eat / Deli
- Hazard
- Affected units
- 75,821
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Date Code Range: 11/22/2019 - 12/06/2019
Distribution
Part of a larger recall action
This product is one of 23 recalled by Fuji Food Products, Inc. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 23 products in this recall →Related recalls
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