CLASS I Food recall · Reported 23 Dec 2020 · FDA Enforcement Report

House Recipe Honey Mustard Dressing & Dip recalled by Treehouse Foods

Treehouse Foods is recalling House Recipe Honey Mustard Dressing & Dip, distributed in Tennessee. The recall was initiated on 3 Dec 2020 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codes81L10050
Quantity recalled511cs/100/1 oz cups

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0189-2021
FDA event ID
86919
Recalling firm
Treehouse Foods, Oak Brook, IL
Classification
Class I
Status
Terminated
Recall initiated
3 Dec 2020
FDA classified
29 Dec 2020
Reported
23 Dec 2020
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Undeclared Milk
Product category
Dips & Spreads

Timeline

3 Dec 2020Recall initiated by company
23 Dec 2020Published in enforcement report+20 days
29 Dec 2020Classified by FDA+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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.

Product as listed by the FDA

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

Where it was distributed

Product was shipped to one customer in TN

Tennessee

Questions about this recall

Why was it 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.

Which lots are affected?

81L10050

Where was it sold?

Product was shipped to one customer in TN

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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