CLASS II Food recall · Reported 7 Dec 2016 · FDA Enforcement Report

Winn Dixie Cream Cheese Creme Cake recalled

Benson's Old Home Kitchens Bakery Division is recalling Winn Dixie Cream Cheese Creme Cake, distributed in 9 states. The recall was initiated on 24 Apr 2016 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes16106
Quantity recalled59,324 units total

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-0535-2017
FDA event ID
73964
Classification
Class II
Status
Terminated
Recall initiated
24 Apr 2016
FDA classified
25 Nov 2016
Reported
7 Dec 2016
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Allergens
Product category
Cakes & Pastries

Timeline

24 Apr 2016Recall initiated by company
25 Nov 2016Classified by FDA+215 days
7 Dec 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

Winn Dixie 32 oz. Cream Cheese Creme Cake

Where it was distributed

AL, DE, FL, LA, NC, OK, SC, TN, TX

AlabamaDelawareFloridaLouisianaNorth CarolinaOklahomaSouth CarolinaTennesseeTexas

Stores named: Winn-Dixie

Questions about this recall

Why was it recalled?

Undeclared allergen; Peanut Protein

Which lots are affected?

16106

Where was it sold?

AL, DE, FL, LA, NC, OK, SC, TN, TX

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

6 other products · FDA event 73964

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