CLASS II Food recall · Reported 18 Oct 2023 · FDA Enforcement Report

Markside Ultimate Peanut Butter Chocolate Cake recalled

Fairfield Gourmet Food is recalling Markside Ultimate Peanut Butter Chocolate Cake (i.e.) Clamp shell, 8 package, Frozen, distributed in 20 states. The recall was initiated on 13 Sep 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLOT # BS23212 (Manufactured on July, 31, 2023)

Quantity recalled120 cASES

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-0010-2024
FDA event ID: 93072
Recalling firm: Fairfield Gourmet Food, Fairfield, NJ
Brand: Markside Ultimate
Classification: Class II
Status: Terminated
Recall initiated: 13 Sep 2023
FDA classified: 11 Oct 2023
Reported: 18 Oct 2023
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Undeclared Allergens
Product category: Cakes & Pastries

Timeline

13 Sep 2023	Recall initiated by company
11 Oct 2023	Classified by FDA	+28 days
18 Oct 2023	Published in enforcement report	+7 days

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

Reason for recall

Fairfield Gourmet Food Corp. d/b/a David s Cookies ,28 Industrial Road, Fairfield NJ 07004has initiated a recall of Markside Ultimate Peanut Butter Chocolate Cake, 7 oz.(198g) plastic package (i.e.) Clamp shell 8 package per case, LOT # BS23212 (Manufactured on July, 31, 2023) because of MISLABELED / UNDECLARED ALLERGENS (Peanuts)

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

Markside Ultimate Peanut Butter Chocolate Cake, 7 oz.(198g), plastic package (i.e.) Clamp shell, 8 package per case, Frozen master case (keep refrigerator Retail pack. LOT # BS23212 (Manufactured on July, 31, 2023).

Where it was distributed

The recall product was distributed to the following states : AL, CA, NV, WA, UT, FL, NM, NC, GA, MO, IL, IN, WI, MN, WY, IN, NE, OK, AR, SC and TN.

Alabama Arkansas California Florida Georgia Illinois Indiana Minnesota Missouri North Carolina Nebraska New Mexico Nevada Oklahoma South Carolina Tennessee Utah Washington Wisconsin Wyoming

Questions about this recall

Why was it recalled?

Which lots are affected?

LOT # BS23212 (Manufactured on July, 31, 2023)

Where was it sold?

The recall product was distributed to the following states : AL, CA, NV, WA, UT, FL, NM, NC, GA, MO, IL, IN, WI, MN, WY, IN, NE, OK, AR, SC and TN.

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.

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