The Recall Desk
Agency classClass IOur severity:SevereFDA (Food)·F-0423-2020·Announced 2020-01-01

Okami brand 8pc Supreme Sampler recalled for potential Listeria monocytogenes contamination

The FDA is recalling Okami brand 8pc Supreme Sampler because products may contain Listeria monocytogenes. No illnesses have been reported, but the recall is classified as FDA Class I.

The agency’s classification

FDA (Food): Class I

Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 4/5 (Severe).

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The recall is classified as FDA Class I, which mandates a minimum severity score of 4 per the rubric. Although no illnesses have been reported, the presence of a high-risk pathogen like Listeria monocytogenes triggers a severe classification.

Plain-English summary

The U.S. Food and Drug Administration is recalling the Okami brand 8pc Supreme Sampler (SKU 28112) because the product may be contaminated with Listeria monocytogenes, a high-risk pathogen. The recall covers all 75,821 units distributed across multiple states including Alabama, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Nebraska, New Hampshire, New Jersey, New York, North Carolina, Ohio, Pennsylvania, Rhode Island, South Carolina, Tennessee, Vermont, Virginia, West Virginia, and Washington D.C.

All units were manufactured by Fuji Food Products, Inc. Consumers are advised to check their inventory and dispose of any remaining product immediately. Those with unopened packages should follow local guidelines for safe disposal. The recall is classified as FDA Class I, indicating a serious health risk requiring immediate consumer action.

The recalled product

Product
Okami brand 8pc Supreme Sampler, SKU 28112
Manufacturer
Fuji Food Products, Inc.
Category
Food — Ready-to-Eat
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

Distributed in 31 states:

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

Same manufacturer · Fuji Food Products, Inc.

See all →

Same hazard · listeria

See all →

Similar recalls