Archive for December, 2010
Drive Total Energy announced today it is voluntarily recalling the company’s Rock Hard Extreme and Passion Coffee Dietary Supplements. Drive Total Energy is conducting the voluntary recall after being informed by the Food and Drug Administration (FDA) that lab analyses found that the products to contain Sulfoaildenafil, an analogue of Sildenafil, an FDA-approved drug used in the treatment of male Erectile Dysfunction (ED), making these products unapproved new drugs. The active drug ingredient is not listed on the product label.
Tags: FDA Recalls
• PRock Marketing LLC, of Kissimmee, Fla., is recalling all lots of Fruta Planta and Reduce Weight Fruta Planta. This is a single product marketed under two brand names.
Tags: fda press release
• PRock Marketing LLC, of Kissimmee, Fla., is recalling all lots of Fruta Planta and Reduce Weight Fruta Planta. This is a single product marketed under two brand names.
Tags: fda press release
Mexicantown Wholesale of Detroit, Michigan is recalling all lots of cuernos (croissants) manufactured between 6/27/2010 and 12/28/2010, because they may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.
Tags: food allergy
Mexicantown Wholesale of Detroit, Michigan is recalling all lots of cuernos (croissants) manufactured between 6/27/2010 and 12/28/2010, because they may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.
Tags: FDA Recalls
Tiny Greens of Urbana, Ill., is recalling all Alfalfa Sprouts and Spicy Sprouts from November 1st thru December 21st because they have the potential to be contaminated with Salmonella. Product was distributed thru various distributors in Illinois, Indiana, and Missouri and could have ended up in restaurants and supermarkets near those areas.
Tags: FDA Recalls
Arrow Intra-Aortic Balloon (IAB) catheters can become stuck in the sheath and potential to cause delay in therapy, bleeding or arterial injury.
Tags: MedWatch Safety Alerts
Following confirmation from regulators of a positive test for
salmonella on curly parsley in Quebec and cilantro in Detroit, J&D Produce Inc. is initiating a
precautionary, voluntary recall of these two items and other potentially affected products packed
only Nov. 30 and Dec. 6, 2010. There have been no reported illnesses.
Tags: FDA Recalls
Nationwide recall initiated December 23 due to some vials of these lots contain particulates.
Tags: MedWatch Safety Alerts
ev3, a Covidien company, has initiated a voluntary recall of specific lots of the NanoCross™ .014″ OTW PTA Dilatation Catheter due to the potential for the catheter shaft to crack or break during use. Cracking or breaking of the catheter shaft may result in the inability to inflate or deflate the balloon, and may result in material separation and potential embolization.
Tags: FDA Recalls