ISH Shrimpish Sample Meal Kit: ( Sample Meal Kit ) a package containing two ISH Foods plant-based Shrimpish products and
Summary
The FDA issued a Class I for ISH Shrimpish Sample Meal Kit: ( Sample Meal Kit ) a package containing two ISH by THE ISH COMPANY. Reason: undeclared soy proteins.
Details
Source
Food Recall
External ID
F-0686-2023
Action Date
2023-04-05
Status
Terminated
Category
food
Product Description
ISH Shrimpish Sample Meal Kit: ( Sample Meal Kit ) a package containing two ISH Foods plant-based Shrimpish products and several additional meal components. Each kit is shipped frozen, using styrofoam and dry ice. Affected components: ¿ Broth Plastic jar with lid ¿ XO Sauce Plastic Jar with lid ¿ Rice Mushroom Grits sealed plastic bag ¿ Breaded Shrimpish Sauce (previously referred to as Mississippi Comeback Sauce) Plastic Jar with Lid
Lot/Code Info: Sample Meal Kits delivered from 2-1-2022 to 12-31-2022; There are no identifying codes on products
Quantity Affected: 355 kits
Reason for Recall
undeclared soy proteins
Distribution
AR, AZ, CA, CO, CT, DC, DE, FL, GA, ID, IL, KS, KY, LA, MA, MD, MI, MN, MO, NC, NH, NJ, NV, NY, OH, OR, PA, PR, SC, TN, TX, UT, VA, VT, WA, WY
Type: Voluntary: Firm initiated
Recall Initiated: 2023-01-09
Company
Greenville, DE
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 66 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (THE ISH COMPANY) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does THE ISH COMPANY have FDA actions?
This is the only FDA action we have on record for THE ISH COMPANY in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0686-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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