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Class ITerminated in FDA datasetRecall initiated Sep 19, 2022

Dutch Red Potatoes with Dijon Mustard Sauce. NET WT. 1 LB 1.7 OZ (502g)

Recalling firm: World Variety Produce Inc dba Melissa's

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Dec 16, 2022.

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Compare the exact product and package details with the label you have.

ProductDutch 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.
Package size1 LB
UPC045255152210

FDA code information

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

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

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.

Extracted codes and context

TypeCode / valueContext
UPC045255152210ch 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.
lotX2599072Lot numbers: X2599072 W0, X2602689 W0. X2603453 W0, X2608167 W0, X2610880 W0, X2611537 W0, X2615737 W0, X2619871 W0, X2624767 W0, X2628160 W0

Original FDA recall reason

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

Recall details

Recall number
F-1810-2022
Event ID
90895
FDA status
Terminated
Initiated
Sep 19, 2022
Reported
Oct 5, 2022
Classified
Sep 29, 2022
Terminated
Dec 16, 2022
Quantity
1701 units
Location
Vernon, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

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

FDA source record · F-1810-2022

Data updated September 16, 2026. View official FDA data ↗

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