Covidien announced that its Mallinckrodt Inc. subsidiary is voluntarily recalling one lot of Mallinckrodt Sodium Chromate Cr-51 Injection, lot #370-9004 as a result of routine post-market testing in which the product was found to be subpotent. Sodium Chromate Cr-51 Injection is a radiopharmaceutical diagnostic agent used in the determination of … [Read more...]
Medtronic Voluntarily Recalls Specific Lots of Paradigm® Quick-Set® Infusion Sets In The United States
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
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
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
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...]
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