Gilster-Mary Lee Corporation Cake Plant Recall: Undeclared egg
United States
TerminatedClass I
- Company
- Gilster-Mary Lee Corporation Cake Plant
- Product
- Bowl & Basket onion soup and dip mix, net wt 2 oz (2-1oz pou…
- Recall date
- November 12, 2024
- Terminated
- February 7, 2025
- Source
- FDA
Reason for recall
Undeclared egg
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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 | 041190083947 | 644 cases | Lot OCT 11 25 E09, Lot SEP 27 25 E07 |
Distribution
- Distributed to one customer in New Jersey
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0148-2025
- Event ID
- 95752
- Status
- Terminated
- Classification
- Class I
- Company
- Gilster-Mary Lee Corporation Cake Plant
- 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
- Quantity
- 644 cases
- Reason
- Undeclared egg
- Recall initiation date
- November 12, 2024
- Report date
- December 4, 2024
- Classification date
- Not published in this source record
- Termination date
- February 7, 2025
- Distribution pattern
- Distributed to one customer in New Jersey
- UPC, lot, and code information
- UPC 041190083947; Lot OCT 11 25 E09, Lot SEP 27 25 E07
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Gilster-Mary Lee Corporation Cake Plant
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
