The Food and Drug Administration is amending its food additive regulations to permit the use in feed and drinking water of animals of selenomethionine hydroxy analogue as a source of selenium in feed for chickens, turkeys, and swine, as well as to provide for the safe use of silicon dioxide as a carrier for selenomethionine hydroxy analogue. Adisseo France filed the underlying petition. The change takes effect March 6.
The Food and Drug Administration took out more than 20 percent of the food facility registrations that were in the agency's database in February, according to a March 4 blog post from Registrar Corp. Registrar said the decrease of some 47,635 "was likely caused by facilities failing to properly renew their registrations before the December 2018 renewal deadline." The FDA removes the registrations soon after the renewal period ends and "as of February 7, 2019, 186,016 food facilities remained in FDA’s database compared to the 233,651 registered in December 2018," the company said. Registrar also posted a registration breakdown by country. The Food Safety Modernization Act requires that food facilities renew FDA registrations during each even-numbered year. "Facilities with expired registrations must re-register with FDA and obtain a new registration number, prior to continuing manufacturing, processing, packing, or storing food for U.S. consumption," Registrar said.
On March 1 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
On Feb. 28 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
On Feb. 27 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
The Food and Drug Administration issued its weekly Enforcement Report for Feb. 27 that lists the status of recalls and field corrections for food, cosmetics, tobacco products, drugs, biologics and devices. The report covers both domestic and foreign firms.
On Feb. 26 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
On Feb. 22 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
On Feb. 21 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
On Feb. 20 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of: