ZENSHI HANDCRAFTED SUSHI Duo Combo - Crunchy CA & Rainbow Roll 10pc Net Wt 8.6oz UPC 0 23012 94206 9
Summary
The FDA issued a Class I for ZENSHI HANDCRAFTED SUSHI Duo Combo - Crunchy CA & Rainbow Roll 10pc Net Wt 8.6oz by Harris Teeter. Reason: Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi..
Details
Source
Food Recall
External ID
H-0153-2025
Action Date
2025-07-09
Status
Terminated
Category
food
Product Description
ZENSHI HANDCRAFTED SUSHI Duo Combo - Crunchy CA & Rainbow Roll 10pc Net Wt 8.6oz UPC 0 23012 94206 9
Lot/Code Info: All lots
Quantity Affected: 5,238 Trays
Reason for Recall
Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
Distribution
Product was shipped to the following states: DC, DE, FL, GA, MD, NC, SC & VA.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-05-20
Company
Matthews, NC
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 154 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Harris Teeter has 85 FDA actions in our database, including 85 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Harris Teeter) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Harris Teeter have FDA actions?
Harris Teeter has 85 FDA actions in our database, including 85 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0153-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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