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12 Aug 2010, 5:59 pm
Food and Drug Administration (FDA), along with Goya Foods, Inc., has announced a precautionary recall of 14 ounce packages of Frozen Mamey Pulp after seven cases of Typhoid, a foodborne illness, in two western states. [read post]
20 Jun 2011, 2:59 am
Food and Drug Administration and San Diego-based Ocean Harvest Inc., together with its president, Minkyu Park, recently signed a consent decree of permanent injunction, the FDA reported last week.The FDA charged that company, an outlet for salmon, tuna, and other fresh fish intended for raw consumption, particularly in sushi, had been selling seafood that was handled in violation of federal food safety standards.The consent decree restrains Ocean… [read post]
4 Feb 2009, 1:26 pm
" The processing "plant in Plainview never was inspected until after the company fell under investigation by the Food and Drug Administration, according to Texas health records obtained by AP. [read post]
24 Nov 2021, 1:50 pm
Fischer & Wieser Specialty Foods is recalling 31.4-ounce jars of H-E-B brand “Creamy Tomato Basil Soup,” according to the company’s recall notice posted by the Food and Drug Administration. [read post]
19 Jul 2015, 10:02 pm
Food and Drug Administration (FDA) sent a formal warning letter June 17, 2015, regarding significant food safety violations to a seafood importer in South El Monte, a city in the San Gabriel Valley in California’s Los Angeles County. [read post]
24 Feb 2022, 12:46 pm
The Food and Drug Administration reported today that the Dublin, OH, company has recalled 15-kilogram — 33-pound — bags of “Yeast Extract Ajirex” packed in boxes because of potential contamination with Salmonella. [read post]
29 May 2008, 5:36 pm
Food & Drug Administration announces your recall on its website, it's not like you really have a choice. [read post]
8 Nov 2022, 12:47 pm
According to the company announcement posted by the Food and Drug Administration, the issue was discovered through routine regulatory testing conducted by the Maryland Department of Health. [read post]
19 Jul 2016, 6:53 pm
Seven brands are included, but only one production code is implicated in the recall of no-salt-added black beans, according to a recall notice posted on the Food and Drug Administration’s website. [read post]
8 Nov 2015, 12:46 pm
Food and Drug Administration (FDA) for use in cat food. [read post]
5 Apr 2019, 12:18 pm
Food and Drug Administration are investigating a multistate outbreak of Shiga toxin-producing E. coli O103 infections. [read post]
15 Dec 2009, 1:59 am
" The Food and Drug Administration (FDA) inspected Seaport Fish on three days last July, and according to an Oct. 14th "Warning Letter" released Dec. 10th, the New Hampshire seafood processing facility has food safety problems with its fresh tuna, cooked lobster and smoked salmon products. [read post]
15 Feb 2013, 10:00 pm
Food and Drug Administration on Friday announced it would extend the public comment period for the information collection provisions associated with two proposed Food Safety Modernization Act rules by three months. [read post]
29 Jul 2022, 9:03 pm
The National Administration of Drugs, Foods and Medical Devices (ANMAT) said a suspected case of botulism has been associated with a product of the A Pleno brand, produced in Villa de las Rosas. [read post]
12 Oct 2023, 9:03 pm
According to an update from the Food and Drug Administration, the outbreak continues to grow, with 67 patients having been confirmed so far. [read post]
11 May 2011, 2:59 am
Food and Drug Administration's office in Beijing. [read post]
30 May 2013, 12:37 am
Food and Drug Administration (FDA) needs to know and food importers need to tell. [read post]
9 Jul 2014, 8:46 pm
The Food and Drug Administration has issued a new warning this June about certain over-the-counter acne medications. [read post]
11 Oct 2019, 8:16 am
Food and Drug Administration (FDA) announced that a technical guidance for industry titled “Bioanalytical Methods Templates” is now available. [read post]
11 Apr 2024, 1:15 pm
The CAFC also affirmed an order of the district court that instructed the Food and Drug Administration (FDA) that the effective approval date of generic company Norwich’s Abbreviated New Drug Application (ANDA) may not precede the expiration dates of the claims of three other Salix patents that were found to be valid and infringed by Norwich. [read post]
