Free Range Grade AA Large White Eggs, Loose Open Skid, 900dz per pallet, Black Sheep Egg Company 400 S Memorial Drive
Summary
The FDA issued a Class I for Free Range Grade AA Large White Eggs, Loose Open Skid, 900dz per pallet, Black by Black Sheep Egg Company, LLC. Reason: Potential Salmonella contamination..
Details
Source
Food Recall
External ID
H-0053-2026
Action Date
2025-10-22
Status
Terminated
Category
food
Product Description
Free Range Grade AA Large White Eggs, Loose Open Skid, 900dz per pallet, Black Sheep Egg Company 400 S Memorial Drive Walnut Ridge AR 72476
Lot/Code Info: Julian Date 190 Sell By: 8/7/2025 through Julian Date 260 Sell By: 10/16/2025
Quantity Affected: 7,200 dozen
Reason for Recall
Potential Salmonella contamination.
Distribution
Retail and wholesale locations in AR and MO Wholesale and broker locations in MS, TX, CA and IN
Type: Voluntary: Firm initiated
Recall Initiated: 2025-09-19
Company
Walnut Ridge, AR
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 75 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Black Sheep Egg Company, LLC has 10 FDA actions in our database, including 10 recalls.
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 (Black Sheep Egg Company, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Black Sheep Egg Company, LLC have FDA actions?
Black Sheep Egg Company, LLC has 10 FDA actions in our database, including 10 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0053-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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