Bowl & Basket onion soup and dip mix, net wt 2 oz (2-1oz pouches), UPC 041190083947, Distributed by: Wakefern Food Corp,
Summary
The FDA issued a Class I for Bowl & Basket onion soup and dip mix, net wt 2 oz (2-1oz pouches), UPC 041190083 by Gilster-Mary Lee Corporation Cake Plant. Reason: Undeclared egg.
Details
Source
Food Recall
External ID
F-0148-2025
Action Date
2024-12-04
Status
Terminated
Category
food
Product Description
Bowl & Basket onion soup and dip mix, net wt 2 oz (2-1oz pouches), UPC 041190083947, Distributed by: Wakefern Food Corp, 5000 Riverside Drive, Keasbey, NJ 08832
Lot/Code Info: Lot OCT 11 25 E09, Lot SEP 27 25 E07
Quantity Affected: 644 cases
Reason for Recall
Undeclared egg
Distribution
Distributed to one customer in New Jersey
Type: Voluntary: Firm initiated
Recall Initiated: 2024-11-12
Company
Perryville, MO
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 82 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Gilster-Mary Lee Corporation Cake Plant) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Gilster-Mary Lee Corporation Cake Plant have FDA actions?
This is the only FDA action we have on record for Gilster-Mary Lee Corporation Cake Plant in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0148-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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