Russ Davis Wholesale product recalled over undeclared allergens

Recall date

February 25, 2019

Source

U.S. Department of Agriculture (USDA FSIS)

Official notice title

Russ Davis Wholesale - Crazy-Fresh Recalls Chicken Products due to Misbranding and Undeclared Allergens

Recall number

021-2019

FDA classification

Class I

Brand / firm

Russ Davis Wholesale, Inc.

Sold / distributed

Iowa

Why it was recalled

Misbranding; Unreported Allergens

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

WASHINGTON, Feb. 25, 2019 Russ Davis Wholesale Crazy-Fresh, an Eagan, Minn. establishment, is recalling approximately 702 pounds of chicken Caesar salad products due to misbranding and undeclared allergens, the U.S. Department of Agricultures Food Safety and Inspection Service (FSIS) announced today. The product contains milk and anchovies, known allergens, which are not declared on the product label. The chicken Caesar salad items were produced from Feb. 11, 2019 through Feb. 22, 2019. The following products are subject to recall: [ View Labels (PDF only)] 10-oz. black plastic bowl with a clear plastic lid containing CRAZY FRESH Chicken Caesar Salad and Use By dates of 02/15/2019 through 02/26/2019 represented on the label. 10-oz. black plastic bowl with a clear plastic lid containing JERRYS the kitchen CHICKEN CAESAR SALAD and SELL BY dates of 02/15/2019 through 02/26/2019 represented on the label. The products subject to recall bear establishment number P-45204 inside the USDA mark of inspection. These items were shipped to retail locations in Iowa, Mich., Minn., Mont., Neb., N.D., S.D., Wis., and Wyo. The problem was discovered on February 24, 2019, when FSIS was notified that the establishment discovered the misbranding of product while performing a label review. 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 consumers refrigerators. 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 that recalling firms are notifying their customers of the recall and that actions are being taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS websit…