CLASS I Food recall · Reported 11 Jan 2023 · FDA Enforcement Report

Culvers Tartar Sauce recalled by Ventura Foods

Ventura Foods is recalling Culvers Tartar Sauce, distributed nationwide in the US. The recall was initiated on 16 Dec 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUse by 04/06/2023
Quantity recalled126 cases, 144 units per case

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-0224-2023
FDA event ID
91347
Recalling firm
Ventura Foods, Brea, CA
Classification
Class I
Status
Terminated
Recall initiated
16 Dec 2022
FDA classified
5 Jan 2023
Reported
11 Jan 2023
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Milk
Product category
Sauces & Condiments

Timeline

16 Dec 2022Recall initiated by company
5 Jan 2023Classified by FDA+20 days
11 Jan 2023Published in enforcement report+6 days

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

Reason for recall

Tartar sauce was found to contain undeclared fish, soy, and milk allergens which was not declared on the label.

Product as listed by the FDA

Culvers Tartar Sauce 2 oz. plastic cups

Where it was distributed

To food service locations throughout the US

Nationwide

Questions about this recall

Is Culvers Tartar Sauce recalled?

Yes. Ventura Foods recalled Culvers Tartar Sauce on 16 Dec 2022. The recall is Class I and its status is Terminated. Recall number F-0224-2023.

Why was it recalled?

Tartar sauce was found to contain undeclared fish, soy, and milk allergens which was not declared on the label.

Which lots are affected?

Use by 04/06/2023

Where was it sold?

To food service locations throughout the US

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 21 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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