RecallHawk
Class I Recall

Everything But The Sushi & Dumplings, 5 fl. oz. (148 mL) glass bottle, UPC 8-60008-58851-7, Made for Seed Ranch Flavor C

Seed Ranch Flavor Co

Summary

The FDA issued a Class I for Everything But The Sushi & Dumplings, 5 fl. oz. (148 mL) glass bottle, UPC 8-600 by Seed Ranch Flavor Co. Reason: Three sauces contain undeclared soy..

Details

Source

Food Recall

External ID

F-0176-2023

Action Date

2022-11-30

Status

Completed

Category

food

Product Description

Everything But The Sushi & Dumplings, 5 fl. oz. (148 mL) glass bottle, UPC 8-60008-58851-7, Made for Seed Ranch Flavor Co., LLC Boulder, CO 80302. Ambient storage - minimum 35 degrees, maximum 85 degrees.

Lot/Code Info: Lot Codes: 071122 081822 6188 BB061025

Quantity Affected: 11,449 bottles

Reason for Recall

Three sauces contain undeclared soy.

Distribution

Nationwide. Canada. UK. France.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-10-20

Company

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 28 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Seed Ranch Flavor Co has 3 FDA actions in our database, including 3 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 (Seed Ranch Flavor Co) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Seed Ranch Flavor Co have FDA actions?

Seed Ranch Flavor Co has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0176-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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