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Top Breaking News
Former Pfizer (PFE) Cancer Scientist Gets All 5 Papers Retracted     4/24/2017
Up to 4,100 Children Victims of Sanofi (SNY)'s Epilepsy Drug, Says French Regulator     4/21/2017
FDA Demands Karyopharm (KPTI) Stop Enrollment of All Selinexor Trials     3/14/2017
Pfizer (PFE)'s Kansas Plant is 'Out of Control' and Puts Patients at Risk, Says the FDA     3/2/2017
Oops, They Did it Again: Theranos Failed to Inform Patients of Potentially Botched Diabetes Test     2/14/2017
Genentech (RHHBY)'s $94,000-a-Year Drug Tarceva: Why Faster FDA Approvals Could Backfire     2/8/2017
FDA Lashes Out at Jazz Pharma (JAZZ) CMO for Continued Regulatory Violations     1/30/2017
Theranos Shuts Down Last Remaining Blood-Testing Lab After Another Failed Inspection     1/19/2017
Sanofi Pasteur (SASY.PA) Abandons Bladder Cancer Drug     11/18/2016
Two Deaths Linked to Bristol-Myers Squibb (BMY)'s Yervoy-Opdivo Combo     11/3/2016
FDA Panel Expresses Concerns Over Allergan (AGN)-Serenity Drug for Nighttime Urination     10/18/2016
Pfizer (PFE) Retracts 5 Articles Authored by Top Cancer Researcher Who Has Since Left the Company     10/14/2016
What You Missed: Nippon Fine Chemical Formed Human Barricade to Stop FDA Employee     10/11/2016
FDA Places Clinical Hold on AML Drug Co-Developed by Johnson & Johnson (JNJ) and Genmab A/S (GEN.CO)     9/20/2016
Flooding Halts Work at GlaxoSmithKline (GSK) Plant     9/16/2016

Featured Stories
Abbott (ABT), Medtronic (MDT) to Withdraw Stents From Indian Market     4/25/2017
Cardiovascular Systems Recalls 900 Saline Infusion Pumps     4/18/2017
Faulty St. Jude Medical (STJ) Devices Were Used in Patients After Recall, Says FDA     4/17/2017
Mylan (MYL)'s Shares Drop After FDA Lashes Out at Drugmaker for Drug Quality Control at HIV Drug Facility     4/12/2017
GlaxoSmithKline (GSK) Is Voluntarily Recalling 593,000 Ventolin Asthma Inhalers     4/5/2017
Mylan (MYL) Expands EpiPen Recall To The U.S.     4/3/2017
Royal Philips Electronics N.V. (PHG)'s HeartStart MRx Recall Is Class I, Says the FDA     3/27/2017
Mylan (MYL) Recalls 81,000 EpiPens Overseas After Reports of Failure     3/23/2017
FDA Warns on Abbott (ABT)’s Bioresorbable Stent     3/21/2017
Medtronic (MDT) Recalls Unused StrataMR Valves and Shunts     3/21/2017
FDA Updates Class I Recall for Medtronic (MDT)’s SynchroMed Drug Pumps     3/15/2017
FDA Slaps a Class I Recall Tag on Physio-Control's Lifepak 1000     3/9/2017
Valeant (VRX) Says It Has Fixed All Issues at Bausch & Lomb Tampa Plant     3/1/2017
Another Theranos Lab Has Blood-Testing License Revoked     2/27/2017
New Findings Show Theranos Repeatedly Violated Its Own Policies     2/9/2017
C. O. Truxton Issues Voluntary Nationwide Recall Of Phenobarbital 15 Mg Tablets, USP Due To Labeling Error On Declared Strength     4/21/2017
FDA Slaps a Class I Tag on Medtronic (MDT)'s HVAD Recall     4/19/2017
UAE Ministry Of Health & Prevention Issues Warning Against Use Of Weight Loss Dietary Supplements & Medical Devices     4/17/2017
CareFusion Recalls IV Sets on Cracked Back-Check Valves     4/14/2017
Abbott (ABT)'s St. Jude Medical (STJ) Unit Hit with FDA Warning Letter on Fortify, Unify, Assura Defibrillators     4/13/2017
FDA Issues Serious Warning on Allergan (AGN)'s IBS Drug Viberzi     3/17/2017
Endo Pharma (ENDP) Issues Voluntary Nationwide Recall For One Lot Of Edex (Alprostadil For Injection) 10 Mcg 2 Pack Carton Due To Potential Lack Of Sterility Assurance     2/27/2017
Boston Scientific (BSX) Sinks After Recalling All Lotus Heart Valves     2/23/2017
Momenta (MNTA) Hit With a Setback After Warning Letter From the FDA     2/20/2017
Zimmer Biomet Recall of Comprehensive Reverse Shoulder System is Class I, Says FDA     2/20/2017
FDA Looks to Block Chinese Surgical Drape Maker Hubei Hongkang Protective Products Over Failed Inspection     2/16/2017
Abbott (ABT) Halts Use of HeartMate PHP Blood Pump After Death, Malfunctions     2/10/2017
CDRH Sending Warning Letters to 3 Foreign Medical Device Manufacturers     2/8/2017
St. Jude Medical (STJ) Discovers New Cardiac Device Flaws, Issues Patch Update     2/8/2017
FDA Slaps a Class I Recall on C.R. Bard's Halo One Thin-Walled Guiding Sheaths     1/31/2017

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