Agri Star Meat And Poultry LLC Recalls Beef Pastrami Products due to Possible Processing Deviation

Recall date

June 21, 2018

Source

U.S. Department of Agriculture (USDA FSIS)

Recall number

052-2018

FDA classification

Class II

Brand / firm

Agri Star Meat and Poultry, LLC

Sold / distributed

California, Florida, Illinois, New York, Washington

Why it was recalled

Processing Defect

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

WASHINGTON, June 21, 2018 Agri Star Meat and Poultry LLC, a Postville, Iowa establishment, is recalling approximately 3,592 pounds of ready-to-eat (RTE) beef pastrami products due to processing deviations that may have led to underprocessing of products and resulted in inadequate curing, the U.S. Department of Agricultures Food Safety and Inspection Service (FSIS) announced today. The RTE beef pastrami items were produced on April 3 and April 4, 2018. The following products are subject to recall: [ View Labels (PDF only)] 21.6-lb. average case weight of fully cooked pastrami that are vacuum-packed using clear plastic and labeled Aarons BEST Beef French Roast Pastrami WATER & CARRAGEENAN PRODUCT. Both the product and the shipping box display a sticker indicating BEST BEFORE 09/10/18. 23.1-lb. average case weight of fully cooked pastrami that are vacuum-packed using clear plastic and labeled SHOR HABOR GLATT KOSHER Beef French Roast Pastrami WATER & CARRAGEENAN PRODUCT. Both the product and the shipping box display a sticker indicating BEST BEFORE 09/11/2018. The products subject to recall bear establishment number EST. 4653A inside the USDA mark of inspection. These items were shipped to distributors in California, Florida, Illinois, New York and Washington. The problem was discovered on June 20, 2018, after the firm received a consumer complaint about product discoloration. The firm conducted an investigation and product testing and determined that not all products contained an adequate amount of the curing solution. The establishment notified FSIS on June 21, 2018. 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. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. FSIS routinely conducts recall effectiveness checks to verify recalling firms…