12 PC Shrimp Tempura Kabuki Roll [WR UPC:81244803410 Products were sold from Genji Sushi counters inside Whole Foods M
Summary
The FDA issued a Class II for 12 PC Shrimp Tempura Kabuki Roll [WR UPC:81244803410 Products were sold from G by Mai Cuisine. Reason: Recall initiated after notification from supplier of recall of frozen shrimp due to Salmonella contamination that had been used in sushi products..
Details
Source
Food Recall
External ID
F-0931-2021
Action Date
2021-09-08
Status
Terminated
Category
food
Product Description
12 PC Shrimp Tempura Kabuki Roll [WR UPC:81244803410 Products were sold from Genji Sushi counters inside Whole Foods Market stores
Lot/Code Info: The products can be identified with the Hand-Crafted date of 8/12/2021 and 8/13/2021 and Best By Date of 08/13/2021 and 08/14/2021
Quantity Affected: 1490 packages - all Genji products
Reason for Recall
Recall initiated after notification from supplier of recall of frozen shrimp due to Salmonella contamination that had been used in sushi products.
Distribution
Northern CA only
Type: Voluntary: Firm initiated
Recall Initiated: 2021-08-13
Company
San Francisco, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 57 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Mai Cuisine has 25 FDA actions in our database, including 25 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (Mai Cuisine) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Mai Cuisine have FDA actions?
Mai Cuisine has 25 FDA actions in our database, including 25 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0931-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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