The U.S. Food and Drug Administration (FDA), the Centers for Disease Control and Prevention (CDC), and the U.S. Department of Agriculture's (USDA) Food Safety and Inspection Service (FSIS) today announced that on Friday, Jan. 10, from 2 to 3 p.m. (EST), they will present a webinar on progress toward attributing foodborne illnesses to food sources. The webinar is open to the public at no charge.
The European Food Safety Authority (EFSA) today published a scientific opinion paper, written by the agency's Panel on Biological Hazards (BIOHAZ), which reviews various molecular typing methods for the four major foodborne pathogens (Salmonella, Escherichia coli, Listeria and Campylobacter) and evaluates the effectiveness of those methods.
Charm Sciences announced Dec. 16 that its ROSA (Rapid One Step Assay) WET (Water Extraction Technology) XR Aflatoxin Quantitative test has received approval from the U.S. Department of Agriculture's (USDA) Grain Inspection, Packers & Stockyards Administration (GIPSA) for the detection, in a single five-minute assay, of 0–100 ppb aflatoxin in feed and grain.
The U.S. Food and Drug Administration (FDA) on Dec.17 extended the period for submission of comments, scientific data and other information related to its draft document titled, “Draft Risk Profile on Pathogens and Filth in Spices.” The new deadline is March 3, 2014.
A new agreement between Marshfield Food Safety, LLC, and PathoGenetix, Inc., provides for independent testing of the RESOLUTION Microbial Genotyping System for use in pathogen confirmation and identification for food industry applications.
The U.S. Food and Drug Administration has decided to extend the comment period by 60 days, to March 8, 2014, on its preliminary determination that partially hydrogenated oils, the primary dietary source of artificial trans fat in processed foods, are not “generally recognized as safe” for use in food.
InstantLabs, a Baltimore-based molecular diagnostic device company, is launching a food safety blog on its website, www.instantlabs.com/blog. The blog will focus on issues related to food safety, micro and molecular biology, lab technique and other topics.
The U.S. Food and Drug Administration (FDA) today is implementing a plan to help phase out the use of medically important antimicrobials in food animals for food production purposes, such as to enhance growth or improve feed efficiency. The plan would also phase in veterinary oversight of the remaining appropriate therapeutic uses of such drugs.
Aspartame and its breakdown products are safe for human consumption at current levels of exposure, EFSA concludes in its first full risk assessment of this sweetener.
Sysco Corp., the nation's biggest foodservice distributor, announced yesterday that it will acquire its largest competitor, US Foods, for $3.5 billion.
A report released today by the U.S. Centers for Disease Control and Prevention details how an outbreak of E. coli O157:H7 in Wisconsin during the 2012 winter holiday season was related to consumption of raw ground beef in specialty items known as "tiger meat" or "cannibal sandwiches."
The U.S. Department of Agriculture has terminated the proposed National Leafy Greens Marketing Agreement, according to an announcement in the December 5 Federal Register.
China Food Safety Testing Industry Report, 2013-2015 — Market Development, Competitive Pattern, Opportunities and Trends
The U.S. Food and Drug Administration (FDA) and the Association of Food and Drug Officials (AFDO) have announced the availability of funds for completion of projects and training to enhance conformance with the Voluntary National Retail Food Regulatory Program Standards (VNRFRPS or Retail Standards).
The U.S. Food and Drug Administration (FDA) on Nov. 21 issued final guidance recommending that primary seafood processors who purchase reef fish such as grouper, amberjack, snapper, lionfish, king mackerel, and barracuda take steps to minimize consumers’ risk of ciguatera fish poisoning (CFP) from the fish they distribute.
The Global Food Safety Initiative (GFSI) has released the first edition of its Food Safety Auditor Competencies on the GFSI website, which are freely available for download by any interested stakeholders. The framework is the culmination of three years of work by the multi?disciplinary GFSI Auditor Competence Working Group, which was mandated by the GFSI Board to define generic food safety auditor competencies underpinning GFSI-benchmarked schemes, and the mechanisms by which they can be assessed and verified.
The U.S. Food and Drug Administration (FDA) today made available its Second Biennial Report to Congress on the Food Emergency Response Network (FERN), as required by Section 202 (b) of the Food Safety Modernization Act (FSMA).
Third-quarter food recalls enforced by the U.S. Food and Drug Administration (FDA) and U.S. Department of Agriculture (USDA) have doubled compared to the second quarter. Supporting data were reported by Stericycle ExpertRECALL in its quarterly ExpertRECALL™ Index.
The U.S. Food and Drug Administration (FDA) today announced the availability of presentations from two recent public meetings about proposed rules on Foreign Supplier Verification Programs and the Accreditation of Third-Party Auditors/Certification Bodies, pursuant to the Food Safety Modernization Act (FSMA).
The U.S. Food and Drug Administration (FDA) is extending the comment period on two proposed rules: “Foreign Supplier Verification Programs for Importers of Food for Humans and Animals” (FSVPs) and “Accreditation of Third-Party Auditors/Certification Bodies to Conduct Food Safety Audits and to Issue Certifications” (Third-Party) that appeared in the July 29, 2013 Federal Register. Comments on these two proposed rules as well as comments on the information collection provisions associated with these rules may be submitted until Jan. 27, 2014. Comments were originally due by Nov. 26, 2013.