CLASS III ONGOING Food recall · Reported 14 Jun 2017 · FDA Enforcement Report

Denali "Original" Moose Tracks Cheesecake recalled by The Father's Table

The Father's Table is recalling Denali "Original" Moose Tracks Cheesecake, distributed in Florida, Georgia. The recall was initiated on 9 May 2017 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot code 1111711/1121731, Exp 04/22/2018, UPC 0-10374-18123-6
Quantity recalled425 cases (9 units per case)

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-2320-2017
FDA event ID
77225
Recalling firm
The Father's Table, Sanford, FL
Brand
Denali
Classification
Class III
Status
Ongoing
Recall initiated
9 May 2017
FDA classified
2 Jun 2017
Reported
14 Jun 2017
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Allergens
Product category
Cakes & Pastries

Timeline

9 May 2017Recall initiated by company
2 Jun 2017Classified by FDA+24 days
14 Jun 2017Published in enforcement report+12 days

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

Reason for recall

Cheesecake has incorrect rear label. The rear label is for Pumpkin Swirl Cheesecake which lacks peanut allergen declaration.

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

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

Where it was distributed

Distributed in Florida and Georgia

FloridaGeorgia

Questions about this recall

Why was it recalled?

Cheesecake has incorrect rear label. The rear label is for Pumpkin Swirl Cheesecake which lacks peanut allergen declaration.

Which lots are affected?

Lot code 1111711/1121731, Exp 04/22/2018, UPC 0-10374-18123-6

Where was it sold?

Distributed in Florida and Georgia

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

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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