Bateman Recalls Poultry Products Due To Misbranding and an Undeclared Allergen

Recall date

August 2, 2017

Source

U.S. Department of Agriculture (USDA FSIS)

Recall number

087-2017

FDA classification

Class I

Sold / distributed

Arizona, California, Oregon

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

EDITORS NOTE (Aug 9, 2017): This release is being reissued to reflect a change in poundage, a new state where the items were shipped and a new lot code. WASHINGTON, Aug. 2, 2017 Bateman, a West Sacramento, Calif. establishment, is recalling approximately 20,638 pounds of poultry products due to misbranding and an undeclared allergen, the U.S. Department of Agricultures Food Safety and Inspection Service (FSIS) announced today. The products contain soy, a known allergen, which is not declared on the product label. 9.1-oz. plastic 3 compartment trays containing CHICKEN with HERB SAUCE POTATOES and CARROTS bearing any of the following Lot Codes: 17817, 14417, 10217, 08617, 05517, 04417, 00217, 36516, 35016, 32816, 30216, 27716, 24316, 22216, and 18216. 9.0-oz. plastic 3 compartment trays containing Bateman Classics Chicken Fillet with Honey Mustard Sauce, Herbed Quinoa, California Blend Vegetables bearing any of the following Lot Codes: 12117, 06717, 04517, 00917, 29516, and 23616. 12.8-oz. plastic 3 compartment trays containing Bateman Classics Chicken Fillet w/ Barbeque Sauce, ROASTED YAMS, GREEN BEANS bearing any of the following Lot Codes: 14617, 08917, 01717, 35616, and 17917. 9.1-oz. plastic 3 compartment trays containing Bateman Classics Chicken Breast Fillet with Apricot Sauce Lemon Quinoa and Brussels Sprouts bearing any of the following Lot Codes: 11117, 06017, 01717, 35516, and 17917. The products subject to recall bear establishment number EST. P45096 inside the USDA mark of inspection. These items were shipped to institutional locations in Arizona, California, and Oregon. The problem was discovered during routine in-plant label verification activities being performed by the company on July 31, 2017. 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 p…