Michael Foods is recalling approximately 4,620 pounds of liquid egg products due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced. The product contains dairy (milk), a known allergen, which is not declared on the product label.
The liquid egg breakfast blend formulation items were produced June 11, 2024, at the company’s facility in Gaylord, Minnesota. The following products are subject to recall:
- 32-oz. paperboard carton containing “FAIR MEADOW Foundations WHOLE EGGS with CITRIC ACID” with the use by date of “16 SEP 24” and lot code 4162G. This product is packaged within a corrugated case labeled Scrambled Egg Blend with the same use by date and lot code.
The products subject to recall bear establishment number “EST. G1455” inside the USDA mark of inspection. These items were shipped to restaurant consignees for institutional use in Alabama, Idaho, Louisiana, Minnesota, Nebraska, New Mexico, Ohio, South Carolina, and Utah.
The problem was discovered during a routine carton inventory evaluation. The establishment notified FSIS when it discovered that a limited amount of Whole Egg with Citric Acid cartons was unaccounted for, and there was a corresponding excess of Breakfast Blend Scrambled Egg carton in inventory. The establishment investigated and determined that the unaccounted Whole Egg with Citric Acid cartons were inadvertently utilized during a single short Breakfast Blend Scrambled Egg production run. The Breakfast Blend formulation contains an allergen, a dairy ingredient (milk), which is not declared on the Whole Egg with Citric Acid label.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
FSIS is concerned that some product may be in institutional/restaurant refrigerators. Restaurants/institutions are urged not to serve these products. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers.
