Food Recall Check
Class I · High risk Terminated Initiated Dec 3, 2020 (6 years ago)

House Recipe Honey Mustard Dressing & Dip recall

Recalled by Treehouse Foods · Oak Brook, IL, United States

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

Why it was recalled

The firm was notified via a consumer complaint that the product contains the Lite Honey Mustard instead of the regular Honey Mustard. The Lite Honey Mustard contains milk which is not listed on the label.

Undeclared allergen: Milk

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

HOUSE RECIPE HONEY MUSTARD DRESSING & DIP NET WT 1 OZ.(28g) cup CONTAINS: EGGS DISTRIBUTED BY SYSCO CORPORATION, HOUSTON, TEXAS 77077 UPC 0 73473 05797 8

Quantity: 511cs/100/1 oz cups

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.

81L10050

Where it was sold

Tennessee

FDA's distribution note: Product was shipped to one customer in TN

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 milk; 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
Treehouse Foods
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 3, 2020
In FDA report of
Dec 23, 2020
Terminated
Feb 24, 2022
FDA recall number
F-0189-2021 · event 86919
Official record
FDA enforcement report search

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