A federal judge in the U.S. District Court for the District of South Dakota yesterday granted the U.S. Food and Drug Administration a permanent injunction against 2035 Inc. and Robert “Larry” Lytle, doing business as QLasers PMA and 2035 PMA.
Category Archives: Food & Drug Recalls
General Mills Issues Voluntary Recall Of Cheerios And Honey Nut Cheerios Cereal Produced At Its Lodi, California Location On Certain Dates
General Mills is voluntarily recalling several days of production of Cheerios and Honey Nut Cheerios cereal produced at its Lodi, California facility on certain dates in July of this year because of an undeclared allergen – wheat – with potential adverse health effects.
Read The Complete Story!
Snack Out Loud Foods Issues Allergy Alert On Undeclared Milk In Snack Out Loud Sea Salt Crunchy Bean Snacks 1.2oz Single Serve Units
Snack Out Loud Foods today announced a recall of 56 cases of Sea Salt Crunchy Bean Snacks labeled with the lot number 63361, UPC 760055900037, Expiration Date 7/9/2016. This recall has been voluntarily initiated due to the possibility of Ranch product being packaged in Sea Salt single-unit serving film, which does not list milk as an allergen. Consumption of this product may cause an allergic reaction to milk. This recall will affect the entire lot identified.
Read The Complete Story!
General Mills Voluntarily Recalls a Limited Quantity of Frozen Cascadian Farm Cut Green Beans
General Mills today announced a voluntary class 2 recall of a limited quantity of frozen Cascadian Farm Cut Green Beans produced on one day in June 2015. The recall is being issued as a precaution after one package of finished product tested positive for the presence of Listeria monocytogenes.
FDA launches national public education campaign to prevent and reduce tobacco use among multicultural youth
The U.S. Food and Drug Administration today announced the launch of a national public education campaign to prevent and reduce tobacco use among youth who identify with the hip-hop peer crowd ‒ a hard-to-reach group that is frequently exposed to pro-tobacco images and messages. The FDA’s new campaign, “Fresh Empire,” is designed to reach the approximately 6 million multicultural youth ages 12–17, specifically African American, Hispanic, and Asian American/Pacific Islander youth, who are open to smoking or are already experimenting with cigarettes.
FDA approves new injectable drug to treat schizophrenia
On October 5, the U.S. Food and Drug Administration approved Aristada (aripiprazole lauroxil) extended release injection to treat adults with schizophrenia. Aristada is administered by a health care professional every four to six weeks using an injection in the arm or buttocks.
FDA approves expanded indication for medical device to treat a form of brain cancer
The U.S. Food and Drug Administration today approved an expanded indication for the Optune device to treat patients with newly-diagnosed glioblastoma multiforme (GBM), an aggressive form of brain cancer. It is given along with the chemotherapy drug temozolomide (TMZ) following standard treatments that include surgery, chemotherapy, and radiation therapy.
FDA approves expanded indication for medical device to treat a form of brain cancer
The U.S. Food and Drug Administration today approved an expanded indication for the Optune device to treat patients with newly-diagnosed glioblastoma multiforme (GBM), an aggressive form of brain cancer. It is given along with the chemotherapy drug temozolomide (TMZ) following standard treatments that include surgery, chemotherapy, and radiation therapy.
K-9 Kraving Dog Food Has Announced a Voluntary Recall of Their Chicken Patties Dog Food Shipped Between July 13th – July 17th, 2015 Because The Product May Be Contaminated With Salmonella and Listeria monocytogenes
K-9 Kraving Dog 13th – July 17th, 2015 because these products may be contaminated with Salmonella and Listeria Food has announced a voluntary recall of their Chicken Patties Dog Food shipped between July Monocytogenes. Salmonella and Listeria Monocytogenes can affect animals eating the products and there is risk to humans from handling contaminated pet products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products.
FDA orders duodenoscope manufacturers to conduct postmarket surveillance studies in health care facilities
The U.S. Food and Drug Administration today ordered the three manufacturers of duodenoscopes marketed in the U.S. to conduct postmarket surveillance studies to better understand how the devices are reprocessed in real-world settings.