Class ITerminatedVoluntary: Firm initiated

Gilster-Mary Lee Corporation Cake Plant: food recall F-0148-2025

Gilster-Mary Lee Corporation Cake Plant of Perryville, MO recalled Bowl & Basket onion soup and dip mix, net wt 2 oz (2-1oz pouches), UPC 041190083947, Distributed by: Wakefern Food… Reason: Undeclared egg. The FDA listed it as Class I in its Enforcement Report dated Dec 4, 2024; distribution: New Jersey.

Record status as published: Terminated (terminated Feb 7, 2025). openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product
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
Product quantity
644 cases
Reason for recall
Undeclared egg
Codes, lots and dates on the package
Lot OCT 11 25 E09, Lot SEP 27 25 E07
Distribution pattern
Distributed to one customer in New Jersey
Recalling firm
Gilster-Mary Lee Corporation Cake Plant, Perryville, MO
Classification
Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Voluntary or mandated
Voluntary: Firm initiated
How the firm first notified customers
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Dates

EventDate
Recall initiated by the firmNov 12, 2024
Classified by the FDANov 25, 2024
Published in the Enforcement ReportDec 4, 2024
TerminatedFeb 7, 2025

All food recall records

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Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0148-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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