FDA Recall United States Terminated Historical recordClass II
The Father's Table, LLC
- Product
- GFS Raspberry Lemonade Cheesecake, 68 oz, 14 cut with papers…
- Published
- August 3, 2016
- Distribution
- In process.
The Father's Table, LLC Recall: Cheesecake has incorrect rear label. The rear label is for Pumpkin Swirl Cheesecake which lacks peanut allergen declaration.
United States
OngoingClass III
- Company
- The Father's Table, LLC
- Product
- Denali "Original" Moose Tracks Cheesecake, Net Wt. 18 oz (51…
- Recall date
- May 9, 2017
- Source
- FDA
Reason for recall
Cheesecake has incorrect rear label. The rear label is for Pumpkin Swirl Cheesecake which lacks peanut allergen declaration.
- - Recall initiated
- - Reported by source
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Denali "Original" Moose Tracks Cheesecake, Net Wt. 18 oz (510g). Black plastic base with clear plastic dome. Back label includes nutrition labeling for Pumpkin Swirl Cheesecake. Manufactured by The Father's Table, LLC | Not published in this source record | 425 cases (9 units per case) | Lot code 1111711/1121731, Exp 04/22/2018, UPC 0-10374-18123-6 |
Distribution
- Distributed in Florida and Georgia
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-2320-2017
- Event ID
- 77225
- Status
- Ongoing
- Classification
- Class III
- Company
- The Father's Table, LLC
- Product description
- Denali "Original" Moose Tracks Cheesecake, Net Wt. 18 oz (510g). Black plastic base with clear plastic dome. Back label includes nutrition labeling for Pumpkin Swirl Cheesecake. Manufactured by The Father's Table, LLC
- Quantity
- 425 cases (9 units per case)
- Reason
- Cheesecake has incorrect rear label. The rear label is for Pumpkin Swirl Cheesecake which lacks peanut allergen declaration.
- Recall initiation date
- May 9, 2017
- Report date
- June 14, 2017
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- Distributed in Florida and Georgia
- UPC, lot, and code information
- Lot code 1111711/1121731, Exp 04/22/2018, UPC 0-10374-18123-6
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: The Father's Table, LLC
Other recalls from The Father's Table, LLC
FDA Recall United States Terminated Historical recordClass II
The Father's Table, LLC
- Product
- GFS Fruit Swirl Variety Cheesecake, 68 oz, 12 cut. Manufact…
- Published
- August 3, 2016
- Distribution
- In process.
FDA Recall United States Terminated Historical recordClass II
The Father's Table, LLC
- Product
- GFS Sea Salt Caramel Cheesecake, 68 oz, 14 cut with papers.…
- Published
- August 3, 2016
- Distribution
- In process.
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 III mean?
A situation in which use of or exposure to a product is not likely to cause adverse health consequences.
Is this recall still active?
According to FDA, this recall's status is "Ongoing." 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?
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