Drug Recall Archives

May29
Xiadafil Recalled By FDA
The U.S. Food and Drug Administration has issued an immediate recall of all Xiadafil VIP Tabs that were sold in 8 tablet bottles( Lot #6K029) or blister packs of two (Lot #6K029-SEI) due to the fact that they contain a potentially...
Feb13
Duragesic Fentanyl Patches Recalled
Duragesic painkiller patches contain fentanyl have been recalled due to a flaw that could cause patients, or even caregivers, to overdose on the drug.Sold by PriCara in the United States and generically by Sandoz Inc the recall includes all 25-micro-gram-per-hour... Continue Reading
Feb 4
Recalled Heparin Causes Allergic Reaction in Dialysis Patients
The Center for Disease Control and Prevention announced that they are investigating 53 incidents of dialysis patients having developed allergic reactions after receiving injections of heparin made by Baxter Healthcare Corp.Last week Baxter voluntarily recalled specific batches of heparin due to... Continue Reading
Jan23
Philippines Joins in Recall of Prexige
On Friday Philippines health regulators, The Bureau of Food and Drugs, ordered Novartis to "immediately initiate a product recall and cease and desist from further importing, distributing, or selling Lumiracoxib (Prexige)".The Philippines joins Australia, who banned the drug in September... Continue Reading
Oct 4
Canada Recalls Prexige from Market
Health Canada announced today that it has stopped all sales of Novartis Pharmaceuticals Canada Inc.'s sale of the anti-inflammatory drug, Prexige.The cancellation of market authorization comes due to the risk of liver related illness such as hepatitis. Health Canada based their... Continue Reading
Sep19
Prexige Recalled in Australia
Australia’s Therapeutic Goods Administration (TGA) has ordered the recall of the anti-inflammatory drug Novartis AG’s Prexige. TGA decided on the recall after the medication was linked to two deaths. Claiming to be the first country to issue the recall, the... Continue Reading
 


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