Intermin data from a study submitted to the FDA by Genentech, makers of the asthma drug Xolair (omalizumab) "suggests a disproportionate increase in ischemic heart disease, arrhythmias, cardiomyopathy and cardiac failure, pulmonary hypertension, cerebrovascular disorders, and embolic, thrombotic and thrombophlebitic events in patients treated with … [Read more...]

Opteron 1 Inc. dba Nature & Health Co., announced today that it is conducting a voluntary nationwide recall of the company's five supplement products sold under the following names: LibieXtreme, Y-4ever, Libimax X Liquid, Powermania Liquid and Capsule, Herbal Disiac. The Company has been informed by representatives of the Food and Drug … [Read more...]

Brookstone Pharmaceuticals, LLC, Alpharetta, GA has initiated a nationwide voluntary recall of all lots of Concentrated Acetaminophen Drops (NDC#42192-504-16) in 16 ounce (473 ml) bulk containers. This 16oz container is comparable to the size generally used to package regular strength acetaminophen liquid preparations. This aspect of the product … [Read more...]

Los Angeles, CA – Haloteco announced today that it is conducting a nationwide voluntary recall of the company's product sold under the name Libipower Plus. Haloteco is conducting this recall after being informed by the representative of the Food and Drug Administration (FDA) that lab analysis of Libipower Plus samples found that the product … [Read more...]

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...]