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Top Breaking News
Boehringer Ingelheim GmbH Withheld Evidence On Blockbuster Blood Thinner     7/24/2014
Baxter International, Inc. (BAX) Initiates Voluntary Worldwide Recall Of Four Lots Of IV Solutions Due To The Presence Of Particulate Matter     7/23/2014
Unique Pharmaceuticals, Ltd. Announces A Voluntary Nationwide Recall Of All Sterile Compounded Preparations Within Their Expiry Period Due To A Lack Of Sterility Assurance     7/21/2014
Baxter International, Inc. (BAX) Initiates Global Recall Of Four Lots Of IV Solutions     7/17/2014
GlaxoSmithKline (GSK) Recalls Painkiller In Puerto Rico     7/16/2014
Sun Pharmaceutical Industries Ltd (SUNPHARMA.NS) Recalls Over 40,000 Bottles Of Antidepressant     7/11/2014
FDA Slaps GlaxoSmithKline (GSK) With Warning For Plant Quality Violations, Orders Company To Review Manufacturing Worldwide     6/26/2014
Dr. Reddy's Laboratories Ltd. (RDY) Recalls Over 13,000 Bottles Of Hypertension Drug     6/20/2014
Mylan Inc. (MYL) Recalls Batches Of Polish-Made Antibiotic: UK     6/19/2014
Hospira, Inc. Announces Voluntary Nationwide Recall Of One Lot Of 0.5% Marcaine™ (Bupivacaine HCI Injection, USP), 30 ML, Single-Dose, Preservative-Free Vial Due To Visible Particulates     6/18/2014
Novartis Pharma K.K. (NVS) Says 10,000 Side Effect Cases Were Never Filed     6/17/2014
Alexion Pharmaceuticals Inc. (ALXN) Initiates Recall Of Certain Lots Of Intravenous Drug Soliris     6/2/2014
Zydus Cadila Recalls Over 10,000 Bottles Of Allergy Drug In U.S.     6/2/2014
FDA Cites Manufacturing Concerns At Wockhardt (WOCKHARDT.BO)'s U.S. Unit     5/28/2014
Fresenius Medical Care Recalls 56 Lots Of Naturalyte® Liquid Bicarbonate Concentrate Due To Potential Health Risk     5/23/2014

Featured Stories
Popular Acne Products Can Be Dangerous, FDA Reveals     6/26/2014
FDA Orders Testosterone Supplement Makers To Include Blood Clot Warnings     6/23/2014
Popular Weight-Loss Supplement Linked to Hepatitis and Liver Failure, USPLabs Reveals     10/11/2013
What Did Mylan Inc. (MYL) Get for $1.6 Billion? A Vaccine Maker With a Troubled Factory     9/25/2013
FDA: 5-Hour Energy Drink Linked to Deaths     11/16/2012
Diabetics in Danger After Drug Sparks Health Alert, Irish Medicines Board Reveals     3/16/2012
Neti Pots Linked to Brain-Eating Amoeba Deaths     12/20/2011
FDA, Federal Trade Commission Act to Remove "Homeopathic" HCG Weight Loss Products from the Market     12/6/2011
GlaxoSmithKline (GSK)'s Avandia - When a Drug is on The Market, But Not Really; Drug Officially Gone From US Pharmacies in November     5/19/2011
AstraZeneca PLC (AZN)'s $6 Billion Stomach Ache: Nexium Causes Bone Fractures     4/22/2011
FDA Says No Fracture Warning Needed for OTC Ulcer Drugs     3/24/2011
US FDA Pulls 500 Unauthorized Prescription Drugs     3/4/2011
FDA Orders New Cautions on Antipsychotic Drugs     2/23/2011
Warning on Danger of Splitting Tablets, Ghent University Study     1/6/2011
Recalled Drugs Tied to Heart Risk Spurs Call for FDA Review     9/29/2010
Cubist Pharmaceuticals, Inc. (CBST) Issues Voluntary Nationwide Recall Of One Lot Of CUBICIN (Daptomycin For Injection) 500 Mg In 10 Ml Single Use Vials Due To Presence Of Particulate Matter     4/18/2014
Trouble for Bliss GVS Pharma Drug in Ghana     10/8/2013
Tobinco to Compensate Customers on the Recall of Gsunate Plus Suppository by FDA     9/17/2013
Fresenius Kabi USA Issues Voluntary Nationwide Recall of Benztropine Mesylate Injection, USP 2 mg/2 mL (1 mg/mL), in 2 mL Single Dose Vials     7/1/2013
Sagent Pharmaceuticals, Inc. Expands a Nationwide Voluntary Recall to All Lots of Vecuronium Bromide for Injection, 10mg Single Use Vials Manufactured by Mustafa Nevzat (MN Pharmaceuticals)     6/13/2013
Novo Nordisk A/S (NVO): Previously Announced FDA Warning Letter Published     2/5/2013
FDA Recalls Hospira, Inc. (HSP)'s Lactated Ringer's and 5% Dextrose Injection, 1000 Ml, Flexible Containers     10/9/2012
Bioniche Life Sciences Inc. (BNC) Discovers a Counterfeit Equine Product     9/24/2012
Bedford Laboratories Broadens Voluntary Recall of Leucovorin Calcium Injection USP     9/18/2012
Qualitest Pharmaceuticals Issues Voluntary, Nationwide Recall for One Lot of Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/500 mg Due to the Potential for Oversized Tablets     9/11/2012
Sun Pharmaceutical Industries Ltd Issues Nationwide Voluntary Recall of One Lot of Nimodipine Capsules Due to Crystallization of the Fill Material     9/4/2012
Bedford Laboratories Issues Nationwide Voluntary Recall of Cytarabine for Injection, USP, 1 Gram Per Vial     2/16/2012
Bedford Laboratories Issues a Voluntary Nationwide Patient Level Recall of Acetylcysteine Solution, USP, Lot 1877093     2/2/2012
Bedford Laboratories Issues Guidance on 2011 Voluntary Recall of Polymyxin B for Injection USP and Vecuronium Bromide for Injection Related to Glass Particulates     1/11/2012
FDA: U.S. Marshals Seize Products Containing Banned Ephedrine for Dietary Supplements     12/7/2011

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