Goot Essa, Der Mutterschaf Cheese, Sheep Tomme Style. 4 and 8 OZ. ( Pasteurized Sheep Milk, Salt, Vegetable Enzymes, Ch
Summary
The FDA issued a Class I for Goot Essa, Der Mutterschaf Cheese, Sheep Tomme Style. 4 and 8 OZ. ( Pasteurized by GOOT ESSA, LLC. Reason: The firm had a positive Listeria Monocytogenes on a sample from this batch of product made..
Details
Source
Food Recall
External ID
H-0647-2025
Action Date
2025-10-08
Status
Ongoing
Category
food
Product Description
Goot Essa, Der Mutterschaf Cheese, Sheep Tomme Style. 4 and 8 OZ. ( Pasteurized Sheep Milk, Salt, Vegetable Enzymes, Cheese Cultures ).
Lot/Code Info: Batch #33, manufactured at plant #26476, exp. 12/24/2025
Quantity Affected: 62 lbs
Reason for Recall
The firm had a positive Listeria Monocytogenes on a sample from this batch of product made.
Distribution
The recalled product was distributed to the following states: CT, NJ, MT, VA
Type: Voluntary: Firm initiated
Recall Initiated: 2025-09-10
Company
Howard, PA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 39 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (GOOT ESSA, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does GOOT ESSA, LLC have FDA actions?
This is the only FDA action we have on record for GOOT ESSA, LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0647-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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