CLASS I Food recall · Reported 5 Oct 2022 · FDA Enforcement Report

Dutch Red Potatoes with Dijon Mustard Sauce recalled

World Variety Produce is recalling Dutch Red Potatoes with Dijon Mustard Sauce, distributed nationwide in the US. The recall was initiated on 19 Sep 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot numbers: X2599072 W0, X2602689 W0. X2603453 W0, X2608167 W0, X2610880 W0, X2611537 W0, X2615737 W0, X2619871 W0, X2624767 W0, X2628160 W0, X2632566 W0

Quantity recalled1701 units

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-1810-2022
FDA event ID: 90895
Recalling firm: World Variety Produce, Vernon, CA
Brand: Dutch
Classification: Class I
Status: Terminated
Recall initiated: 19 Sep 2022
FDA classified: 29 Sep 2022
Reported: 5 Oct 2022
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Undeclared Egg
Product category: Sauces & Condiments

Timeline

19 Sep 2022	Recall initiated by company
29 Sep 2022	Classified by FDA	+10 days
5 Oct 2022	Published 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

Dutch Red Potatoes were packed with a Dijon Mustard Sauce packet that did not declare the allergen of egg.

Product as listed by the FDA

Dutch Red Potatoes with Dijon Mustard Sauce. NET WT. 1 LB 1.7 OZ (502g) UPC code 0-45255-15221-0 Distributed by World Variety Produce, Inc. Los Angeles, CA Product of USA.

Where it was distributed

NATIONWIDE (Arizona, California, Florida, Iowa, Idaho, Kansas, Louisiana, Mississippi, Montana, New Jersey, Oklahoma, Pennsylvania, Texas, Utah, Washington)

Nationwide Arizona California Florida Iowa Idaho Kansas Louisiana Mississippi Montana New Jersey Oklahoma Pennsylvania Texas Utah Washington

Questions about this recall

Why was it recalled?

Dutch Red Potatoes were packed with a Dijon Mustard Sauce packet that did not declare the allergen of egg.

Which lots are affected?

Lot numbers: X2599072 W0, X2602689 W0. X2603453 W0, X2608167 W0, X2610880 W0, X2611537 W0, X2615737 W0, X2619871 W0, X2624767 W0, X2628160 W0, X2632566 W0

Where was it sold?

NATIONWIDE (Arizona, California, Florida, Iowa, Idaho, Kansas, Louisiana, Mississippi, Montana, New Jersey, Oklahoma, Pennsylvania, Texas, Utah, Washington)

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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