Saker Shoprites product recalled over undeclared allergen

Recall date

February 14, 2018

Source

U.S. Department of Agriculture (USDA FSIS)

Official notice title

Saker ShopRites, Inc. Recalls Empanadas due to Misbranding and an Undeclared Allergen

Recall number

010-2018

FDA classification

Class I

Brand / firm

Saker Shoprites Inc

Sold / distributed

New Jersey

Why it was recalled

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. 14, 2018 Saker ShopRites, Inc., a Linden, N.J. establishment, is recalling approximately 19,757 pounds of pork and chicken empanadas due to misbranding and an undeclared allergen, the U.S. Department of Agricultures Food Safety and Inspection Service (FSIS) announced today. The products contain egg, a known allergen, which is not listed in the ingredient statement on the label. The fully cooked pork and chicken empanadas were produced between Oct. 7, 2017 and Feb. 12, 2018. There have been no reports of injuries. The following products are subject to recall: [ View Labels (PDF Only)] 9-oz. vacuum-packed plastic packages containing three pieces of 3 pk CHICKEN EMPANADA wheat shell filled with seasoned chicken with various expiration dates between Oct. 15, 2017 and Feb. 20, 2018. 6-oz. vacuum-packed plastic packages containing three pieces of 2 pk CHICKEN EMPANADA wheat shell filled with seasoned chicken with various expiration dates between Oct. 15, 2017 and Feb. 20, 2018. 9-oz. vacuum-packed plastic packages containing three pieces of 3 pk PORK EMPANADA wheat shell filled with seasoned pork with various expiration dates between Oct. 15, 2017 and Feb. 20, 2018 6-oz. vacuum-packed plastic packages containing three pieces of 2 pk PORK EMPANADA wheat shell filled with seasoned pork with various expiration dates between Oct. 15, 2017 and Feb. 20, 2018. The products subject to recall bear establishment number EST. 5495 or EST. P-5495 inside the USDA mark of inspection. These items were shipped to retail locations in New Jersey. The problem was discovered by FSIS personnel during routine label verification activities. 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…