U.S. Food & Drug Administration (FDA)


03/20/2013 09:24 PM EDT
Tinton Falls, NJ., Med Prep Consulting, Inc. is voluntarily recalling all lots of all products compounded at its facility. The level of recall is to the user, that is, regional hospital pharmacies and related departments, and physicians office practices. The recall resulted from the pharmacy being notified by a Connecticut hospital, that it observed visible particulate contaminants in 50 ml bags of MAGNESIUM SULFATE 2GM IN DEXTROSE 5 Percent IN WATER, 50ML FOR INJECTION intravenous solution confirmed to be mold.
03/20/2013 07:11 PM EDT
New Chapter, Inc. is voluntarily recalling a limited number of packages of its 90 count Probiotic Elderberry dietary supplement because it may contain an undeclared allergen – soy.  People who have an allergy or severe sensitivity to soy run the risk of serious or life-threatening allergic reaction if they consume this product.
03/20/2013 09:22 PM EDT
Clinical Specialties is voluntarily recalling All Lots of All Sterile products repackaged and distributed by the pharmacy due to lack of sterility assurance. The recall of all sterile products is conducted in follow-up to concerns regarding practices at the site which cannot assure the sterility of the products. The expanded recall follows the firms initial recall of Avastin due to reports of five patients who have been diagnosed with serious eye infections associated with the use of the product.
March 19, 2013 – Daesang America Inc. One University Plaza, Suite 603, Hackensack, NJ 07601 is recalling its 500gram (17.64 Ounce) packages of Sesame and Garlic flavored Mixed Soy Bean Paste because they may contain undeclared peanuts. People who have allergies to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.
03/20/2013 03:04 PM EDT
La Preferida, Inc. is voluntarily recalling 4,734 cases (56,808 cans) of La Preferida Whole Pinto Beans 29 oz. (Water & Salt). Can Code: PINTO LP, BEST BY 01/03/2015, “Time” 3003. The manufacturer’s preliminary inspection indicates 420 cans may not have been fully processed, which could result in product contamination by spoilage organisms or by pathogens, which could lead to illness if consumed.