Food Recall Check
Class I · High risk Completed Initiated Oct 20, 2022 (4 years ago)

Everything But The Sushi & Dumplings recall

Recalled by Seed Ranch Flavor Co · Boulder, CO, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Three sauces contain undeclared soy.

Undeclared allergen: Soy

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

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.

Quantity: 11,449 bottles

Food: Salads, sandwiches & prepared foods

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot Codes: 071122 081822 6188 BB061025

Where it was sold

Nationwide.

FDA's distribution note: Nationwide. Canada. UK. France.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to soy; for anyone else the product is generally not a safety concern. FDA lists this recall as completed: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Seed Ranch Flavor Co
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 20, 2022
In FDA report of
Nov 30, 2022
FDA recall number
F-0176-2023 · event 91042
Official record
FDA enforcement report search

Also recalled with it (2 more products)

FDA files each product of one recall action separately; these share the same FDA event.

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