RecallHawk
Class I Recall

ISH Shrimpish Sample Meal Kit: ( Sample Meal Kit ) a package containing two ISH Foods plant-based Shrimpish products and

THE ISH COMPANY

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

THE ISH 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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