Boa Vida Imports Recalls Pork And Beef Products Imported From An Ineligible Country Without Benefit Of Import Inspection

Recall date

March 20, 2015

Source

U.S. Department of Agriculture (USDA FSIS)

Recall number

050-2015

FDA classification

Class I

Sold / distributed

Massachusetts

Why it was recalled

Import Violation

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, March 20, 2015 Boa Vida Imports, a New Bedford, Mass., establishment, is recalling approximately 385 pounds of pork and beef products imported from Portugal because this country is not eligible to export meat products to the United States, the U.S. Department of Agricultures Food Safety and Inspection Service (FSIS) announced today. These products were also not presented at the U.S. point of entry for inspection. Without the benefit of full inspection, including determining the equivalence of a foreign food regulatory system, a possibility of adverse health consequences exists. The pork meat and beef tripe stew with beans items were produced on various dates between July and October 2014. The following products are subject to recall: [ View Labels (pdf only)] 1-lb. cans of NOBRE Receitas Caseiras CHISPALHADA with a use or sell by date of 10/21/2016 on the can. 1-lb. cans of NOBRE Receitas Caseiras DOBRADA COM FEIJAO BRANCA with a use or sell by date of 09/23/2016 on the can. 1-lb. cans of NOBRE Receitas Caseiras FEIJOADA A TRANSMOTANA with a use or sell by date of 07/10/2016 on the can. The products subject to recall bear the establishment number PT RTR 79 CE inside the Portugal mark of inspection. These products were shipped to retail locations in Southeastern Massachusetts. The problem was discovered when Animal and Plant Health Inspection Service (APHIS) contacted a FSIS Office of Investigation, Enforcement, and Audit (OIEA) Investigator on the suspicion that these products were imported from a country (Portugal) not currently eligible for import. FSIS and the company have received no reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider. 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. When available, the ret…