Deseo Rebajar Inc. está recogiendo voluntariamente el lote# MFD: 07.18.2013 (Exp: 07.17.2015) del producto Burn 7. Pruebas de laboratorio del FDA encontraron que este suplemento dietético contenía el ingrediente activo Sibutramina sin declarar.
Voluntary Field Corrective Action Initiated for Vital Signs Device’s CO2 Multi Absorber Due to a Health Risk
Vital Signs Devices, a GE Healthcare Company, has initiated a voluntary field corrective action of the disposable Multi Absorber Original after becoming aware of a potential safety issue due to air leakage associated with the CO2 Multi Absorber. The Multi Absorber Original may have a thin wall condition which may lead to small holes in the water (drain tube). This may result in a loss of anesthetic gases, ventilation and oxygenation.
Campbell Recalls 300 Cases of Prego Traditional Italian Sauce Due to a Risk of Spoilage
Campbell Soup Company is voluntarily recalling approximately 300 cases of 24-ounce jars of Prego Traditional Italian sauce because of a risk of spoilage. The affected product was manufactured on December 15, 2013 and can be identified by the Best By date of June 16, 2015 and a four-digit, military time code ranging from CT BJ ZV 0330 through CT BJ ZV 0449.
The Cultured Kitchen Voluntarily Recalls Cashew Cheese Due To Possible Risk Of Contamination From Salmonella
The Cultured Kitchen of West Sacramento, CA is voluntarily recalling all flavors of their non-dairy cashew cheese product due to a risk of contamination from Salmonella. The non-dairy cashew cheese was distributed in Northern California and Nevada at various natural foods stores and farmers markets in the Sacramento Valley, San Francisco Bay Area, and Reno.
Zip International Group LLC Recalls FOSFOREL Herring Fillet in Oil Due to Potential Health Risk
ZIP INTERNATIONAL GROUP LLC, 160 Raritan Center Parkway #6, Edison, NJ 08837, is recalling herring fillet in oil (FOSFOREL, ATLANTIKA) 200 grams in plastic packaging due to Listeria contamination.
Giant Eagle Issues Allergy Alert On Undeclared Peanut Allergen In Candy Place Chocolate Santas
Candy Place Chocolate Santas packages were voluntarily recalled by Giant Eagle due to an undeclared peanut allergen. While the individual peanut butter filled candies reference “peanut butter�, peanuts are not listed as an ingredient on the primary package label, creating the potential for a serious or life-threatening allergic reaction if consumed by those with a peanut allergy. The product is safe for consumption by those who do not have a peanut allergy.
Baxter Initiates Worldwide Voluntary Recall Of Select Lots Of 5 percent Dextrose Injection, USP And 0.9 percent Sodium Chloride Injection, USP Intravenous (IV) Solutions
Baxter International Inc. announced today it has initiated a voluntary recall to the hospital/user level of one lot of 5 percent Dextrose Injection, USP and four lots of 0.9 percent Sodium Chloride Injection, USP due to particulate matter found in the solutions. Injecting a product containing particulate matter may result in blockages of blood vessels, which can result in stroke, heart attack or damage to other organs such as the kidney or liver.
Deseo Rebajar Inc. Issues Voluntary Recall of Burn 7 Capsules Due to Undeclared Active Ingredient
Deseo Rebajar Inc., is voluntarily recalling lot #MFD: 07.18.2013 (Exp: 07.17.2015) of Burn 7 Capsules to the consumer level. The FDA laboratory analysis of this dietary supplement found the Burn 7 Capsules product to contain undeclared Sibutramine.
FDA warns consumers not to use muscle growth product
The U.S. Food and Drug Administration is advising consumers to immediately stop using a product called Mass Destruction, marketed as a dietary supplement for muscle growth. The product is labeled to contain at least one synthetic anabolic steroid and has been linked to at least one reported serious illness.
FDA approves Tretten to treat rare genetic clotting disorder
The U.S. Food and Drug Administration today approved Tretten, Coagulation Factor XIII A-Subunit (Recombinant), the first recombinant product for use in the routine prevention of bleeding in adults and children who have a rare clotting disorder, known as congenital Factor XIII A-subunit deficiency.