Kagome Worchester Sauce
Reason Products contain soy that is not declared on the label.
Kagome Chuno Sauce recall
Recalled by North American Food Dist. Co., Inc. · West Sacramento, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Products contain soy that is not declared on the label.
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
Kagome Chuno Sauce 16.9 fl., oz plastic bottles
Quantity: 125 bottles
Food: Sauces, dips & dressings
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.
UPC code is 4901306097519
Where it was sold
California Colorado Nevada
FDA's distribution note: U.S. distribution to the following: CA, CO, NV
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 terminated: 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
- North American Food Dist. Co., Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 27, 2023
- In FDA report of
- Apr 26, 2023
- Terminated
- Aug 13, 2025
- FDA recall number
- F-0737-2023 · event 91976
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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