Tag Archives: Potato chip

~ FDA/USDA ~~ Alerts & Safety

U.S. Food & Drug Administration (FDA)


Wethepeople
03/15/2013 07:44 PM EDT
Nishimoto Trading Co., Ltd of Santa Fe Springs, CA, is recalling its 4.37 ounce packages of Kameda Brand Rice Cracker “Kotsubukko” snack food because they may contain undeclared milk. People who have allergies to milk run the risk of serious or life-threatening allergic reaction if they consume these products.
03/15/2013 07:24 PM EDT
Grippo Foods, Inc, Cincinnati, OH, is initiating a nationwide recall of all bags and boxes of their Plain Potato Chips, Bar-B-Q Potato Chips, Cheddar Cheese with a touch of Jalapeno Potato Chips, Hot Dill Pickle Potato Chips, Sweet Bermuda Onion Potato chips and Salt & Vinegar Potato Chips. These products may have the potential to contain metal fragments.
03/15/2013 07:35 PM EDT
On February 28, 2013, Vascular Solutions Zerusa Ltd., a subsidiary of Vascular Solutions, Inc., initiated a nationwide recall of Guardian® II and Guardian II NC hemostasis valves used in catheterization procedures. Specific lots of the products have been recalled because they pose a slightly increased risk of air leakage that may lead to an air embolism, which could result in serious injury or death.
03/17/2013 08:49 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 physician’s 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.
03/16/2013 08:52 PM EDT
Tinton Falls, NJ., Med Prep Consulting, Inc. is voluntarily recalling all lots of Magnesium Sulfate 2 grams in Dextrose 5 percent for Injection products compounded at its facility. The level of recall is to the user, that is, regional hospital pharmacies and related departments. 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.Â