CLASS II Food recall · Reported 3 Aug 2016 · FDA Enforcement Report

GFS Brownie Cheesecake, 12 cut with papers recalled

The Father's Table is recalling GFS Brownie Cheesecake, 12 cut with papers. The recall was initiated on 20 Jun 2016 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesItem #: 75664, Package/Case # (exp date): 1231642/05-02-17 (05/02/17).
Quantity recalled156 cases (624 cakes)

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-1826-2016
FDA event ID
74521
Recalling firm
The Father's Table, Sanford, FL
Classification
Class II
Status
Terminated
Recall initiated
20 Jun 2016
FDA classified
22 Jul 2016
Reported
3 Aug 2016
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Allergens
Product category
Cakes & Pastries

Timeline

20 Jun 2016Recall initiated by company
22 Jul 2016Classified by FDA+32 days
3 Aug 2016Published 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

Undeclared allergen- peanut protein.

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

GFS Brownie Cheesecake, 54 oz, 12 cut with papers. Manufactured by The Fathers Table and Distributed by Gordon Food Service.

Where it was distributed

In process.

Questions about this recall

Why was it recalled?

Undeclared allergen- peanut protein.

Which lots are affected?

Item #: 75664, Package/Case # (exp date): 1231642/05-02-17 (05/02/17).

Where was it sold?

In process.

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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.

Other products in this recall event

5 other products · FDA event 74521

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