As of Sept. 30, 2019, the U.S. Food and Drug Administration (FDA) has tested 1,214 fresh herb samples (746 domestic, 468 imported). And as of Oct. 15, 2019, the FDA has tested 887 processed avocado or guacamole samples (777 domestic, 110 imported).
Of the fresh herb samples, 13 tested positive for Salmonella (four domestic, nine imported), and nine tested positive for Shiga-toxin producing E. coli (STEC) (four domestic, five imported). Further study showed that the STEC were incapable of causing severe illness.
The FDA did not detect E. coli O157:H7 in any of the fresh herb samples. The agency also began testing its fresh herb samples for Cyclospora cayetanensis in July 2018, given that Cyclospora-related illnesses typically occur during the summer. The agency detected Cyclospora in 16 of the 666 fresh herbs samples tested (four domestic, 12 imported). The FDA continues to test more herb samples, so no conclusions can be drawn at this time.
Of the processed avocado or guacamole samples, 15 tested positive for Listeria monocytogenes (13 domestic, two imported), and two tested positive for Salmonella (both domestic samples). The FDA concluded its collection of processed avocado and guacamole samples with the close of fiscal year 2019. The FDA has recently begun its analysis of the processed avocado and guacamole samples, and the results will be published in the final report.
Scientists from the USDA's Agricultural Research Service (ARS) have identified a new way to detect the presence of live African Swine Fever Virus (ASFV) that minimizes the need for samples from live animals and provides easier access to veterinary labs that need to diagnose the virus.
The report, prepared by USDA’s Agricultural Marketing Service in coordination with the Office of the Chief Economist, summarizes market conditions, fed cattle prices, boxed beef values, and the spread before and after the fire and plant closure at the Tyson Holcomb, Kan., plant, and before and during the COVID-19 pandemic.
The European Food Safety Authority (EFSA) has released a draft approach that aims to harmonize assessments of the intake of these nutrients, the potentially hazardous properties of excessive intakes, and the overall risks for consumers.
The U.S. Food and Drug Administration (FDA) has announced that routine inspections of small businesses to verify compliance with the FDA Food Safety Modernization Act’s (FSMA) Intentional Adulteration (IA) rule will begin in March 2021.
On July 13, Stephen M. Hahn, commissioner for the U.S. Food and Drug Administration (FDA), announced the release of the New Era of Smarter Food Safety blueprint.
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