CLASS I Food recall · Reported 4 Dec 2024 · FDA Enforcement Report

Bowl & Basket onion soup and dip mix recalled

Gilster-Mary Lee Corporation Cake Plant is recalling Bowl & Basket onion soup and dip mix, distributed in New Jersey. The recall was initiated on 12 Nov 2024 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot OCT 11 25 E09, Lot SEP 27 25 E07
Quantity recalled644 cases

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-0148-2025
FDA event ID
95752
Recalling firm
Gilster-Mary Lee Corporation Cake Plant, Perryville, MO
Brand
Bowl
Classification
Class I
Status
Terminated
Recall initiated
12 Nov 2024
FDA classified
25 Nov 2024
Reported
4 Dec 2024
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Egg
Product category
Soup

Timeline

12 Nov 2024Recall initiated by company
25 Nov 2024Classified by FDA+13 days
4 Dec 2024Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared egg

Product as listed by the FDA

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

Where it was distributed

Distributed to one customer in New Jersey

New Jersey

Questions about this recall

Why was it recalled?

Undeclared egg

Which lots are affected?

Lot OCT 11 25 E09, Lot SEP 27 25 E07

Where was it sold?

Distributed to one customer in New Jersey

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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