FDA Press Releases Archives - Page 783 of 803

Medtronic Voluntarily Recalls Specific Lots of ParadigmÂ® Quick-SetÂ® Infusion Sets In The United States

July 1, 2009 By The FDA Leave a Comment

UPDATED URL > Click Here for information on the Medtronic Paradigm Quick Set Infusion Set Recall … [Read more...]

Hi-Tech Pharmaceuticals Recalls All Lots of Stamina-Rx Dietary Supplement Products

June 17, 2009 By The FDA Leave a Comment

Norcross, GA - Hi-Tech Pharmaceuticals, Inc. ("Hi-Tech"), 6015-B Unity Dr., Norcross, GA 30071, announced today that it is conducting a nationwide voluntary recall of the company's product sold under the name Stamina-Rx. On May 1, 2009, Hi-Tech was notified by the Food and Drug Administration (FDA) that FDA's lab analysis of one lot of Stamina-Rx … [Read more...]

Zicam Recall Information

June 16, 2009 By E. Sizemore 6 Comments

UPDATE: A Zicam recall is being conducted voluntarily by Matrixx, makers of Zicam Cold Remedy products. FDA is warning consumers about certain Zicam products and a troubling potential side effect: loss of sense of smell. According to the FDA warning, they have received over 130 reports of loss of smell from consumers who associated the side … [Read more...]

FoodScience Corporation Recalls Kid's Multivitamin for Label Error

June 10, 2009 By The FDA Leave a Comment

FoodScience Corporation of Essex Junction, Vermont 05452 is voluntarily recalling a total of approximately 1,250 bottles of its Children's Multi Vitamins. The recall was initiated after it was discovered during the revising of product labels for reprint, that there was an error on the labels' suggested use recommendation. The label currently … [Read more...]