Dutch Red Potatoes with Dijon Mustard Sauce. NET WT. 1 LB 1.7 OZ (502g) UPC code 0-45255-15221-0 Distributed by World
Summary
The FDA issued a Class I for Dutch Red Potatoes with Dijon Mustard Sauce. NET WT. 1 LB 1.7 OZ (502g) UPC co by World Variety Produce Inc dba Melissa's. Reason: Dutch Red Potatoes were packed with a Dijon Mustard Sauce packet that did not declare the allergen of egg..
Details
Source
Food Recall
External ID
F-1810-2022
Action Date
2022-10-05
Status
Terminated
Category
food
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.
Lot/Code Info: Lot numbers: X2599072 W0, X2602689 W0. X2603453 W0, X2608167 W0, X2610880 W0, X2611537 W0, X2615737 W0, X2619871 W0, X2624767 W0, X2628160 W0, X2632566 W0
Quantity Affected: 1701 units
Reason for Recall
Dutch Red Potatoes were packed with a Dijon Mustard Sauce packet that did not declare the allergen of egg.
Distribution
NATIONWIDE (Arizona, California, Florida, Iowa, Idaho, Kansas, Louisiana, Mississippi, Montana, New Jersey, Oklahoma, Pennsylvania, Texas, Utah, Washington)
Type: Voluntary: Firm initiated
Recall Initiated: 2022-09-19
Company
Vernon, CA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 76 food recalls issued in the same week, part of 204 food-related FDA actions this month.
World Variety Produce Inc dba Melissa's has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (World Variety Produce Inc dba Melissa's) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does World Variety Produce Inc dba Melissa's have FDA actions?
World Variety Produce Inc dba Melissa's has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1810-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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