RecallRadar
FDA · FoodClass I

Goot Essa, LLC food recall: Goot Essa

Listeria

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Terminated
Event ID
97642
Recall initiated
Sep 10, 2025
Classified by FDA
Sep 30, 2025
Posted in Enforcement Report
Oct 8, 2025
Terminated
Oct 30, 2026
Recalling firm
GOOT ESSA, LLC
Firm location
Howard, PA, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Products in this event
1

What to do

Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.

View the official FDA record ↗

Reason for recall

The firm had a positive Listeria Monocytogenes on a sample from this batch of product made.

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Sep 10, 2025. FDA classified it 20 days later, on Sep 30, 2025. Distribution reported by FDA: The recalled product was distributed to the following states: CT, NJ, MT, VA

Recalled products (1)

  • H-0647-2025 Class I Terminated

    Goot Essa, Der Mutterschaf Cheese, Sheep Tomme Style. 4 and 8 OZ. ( Pasteurized Sheep Milk, Salt, Vegetable Enzymes, Cheese Cultures ).

    Codes / lots: Batch #33, manufactured at plant #26476, exp. 12/24/2025

    Quantity: 62 lbs

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
Official notice
FDA Enforcement Report, event 97642
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.