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Zold - Biotech/Pharma - FDA - Medwatch
MedWatch Watson Pharmaceuticals, Inc. (WPI) Announces a Nationwide Voluntary Recall of Propafenone HCL Tablets Due to Oversized Tablets 3/27/2009
MedWatch: Welch Allyn AED 10 and and MRL JumpStart Defibrillators 3/19/2009
MedWatch: FDA Warns Risk of Transmission of Blood-borne Pathogens from Shared Use of Insulin Pens 3/19/2009
MedWatch: Class 1 Recall: Baxter Healthcare Corporation (BAX) Colleague Single and Triple Channel Volumetric Infusion Pumps 3/13/2009
MedWatch: Class 1 Recall: Covidien Inc., Shiley 3.0PED Cuffless Pediatric Tracheostomy Tube 3/13/2009
MedWatch: Safety Labeling Changes Approved By FDA Center for Drug Evaluation and Research 3/13/2009
MedWatch: FDA Requires Boxed Warning and Risk Mitigation Strategy for Metoclopramide-Containing Drugs 3/5/2009
MedWatch: FDA Public Health Advisory Risk of Burns during MRI Scans from Transdermal Drug Patches with Metallic Backings 3/5/2009
MedWatch: March 2009 Patient Safety News 3/5/2009
MedWatch: Information for Healthcare Professionals for Zonisamide 2/25/2009
MedWatch: FDA Early Communication about an Ongoing Safety Review Xigris 2/25/2009
MedWatch: FDA Public Health Advisory Updated Safety Information about Raptiva 2/25/2009
MedWatch: ETHEX Corporation (KVa) Product Recall 2/12/2009
MedWatch: FDA and Roche Laboratories Introduce CellCept Medication Guide 2/12/2009
MedWatch: Early Communication About An Ongoing Safety Review of Xigris 2/12/2009
MedWatch: FDA to Conduct Safety Review to Evaluate Plavix 1/27/2009
MedWatch: FDA Public Health Advisory: Potential Hazards of Skin Products Containing Numbing Ingredients for Relieving Pain from Mammography and Other Medical Tests and Conditions 1/27/2009
MedWatch: Update of Safety Review of Montelukast (Singulair) 1/27/2009
MedWatch: Update of Safety Review for Vytorin, Zetia, and Zocor 1/9/2009
MedWatch: FDA Announces Hydromorphone HCl 2 mg Tablets Nationwide Recall 1/6/2009
MedWatch: Stryker Corporation  (SYK) Craniomaxillofacial Issues Nationwide Recall of its Custom Cranial Implant Kits 1/6/2009
MedWatch: FDA Announces Innohep (tinzaparin sodium injection) Update 1/6/2009
MedWatch: FDA Issues Weight Loss Pills Recall 12/23/2008
MedWatch: Oral Sodium Phosphate (OSP) Products for Bowel Cleansing Products Available without a Prescription 12/23/2008
MedWatch: Sun Med and FDA Announce Class 1 Recall of Greenline/D MacIntosh No. 3 Laryngoscope Blades 12/23/2008
MedWatch: Class 1 Recall: Integra NeuroSciences Gravity Compensating Accessory 12/11/2008
MedWatch: Class 1 Recall: Advanced Medical Optics, Inc. (EYE) Healon D Ophthalmic Viscosurgical Device (OVD) 12/11/2008
MedWatch: Communication about an Ongoing Safety Review of Innohep (tinzaparin sodium injection) 12/9/2008
MedWatch: Terumo Cardiovascular Systems Issues Urgent, Nationwide/Worldwide Recall of Pediatric Arterial Cannulae 12/9/2008
MedWatch: Phenytoin and Fosphenytoin Sodium Updates 11/24/2008
MedWatch: Class 1 Recall of Animas Corporation Battery Caps Used with the OneTouch Ping System, Animas 2020 Insulin Pump, Animas IR1200 Insulin Pump, and Animas IR1250 Insulin Pump 11/20/2008
MedWatch: Benzoyl Peroxide Acne Cream 10%: Product Recalled 11/17/2008
Johnson & Johnson (JNJ), Merck Consumer Pharmaceuticals Company Announces Urgent Voluntary Nationwide Recall Of Infants' Mylicon Gas Relief Dye Free Drops 11/17/2008
Update of Safety Review Follow-up to the October 1, 2007 Early Communication about the Ongoing Safety Review of Bisphosphonates 11/12/2008
ETHEX Corporation (KVa) Initiated Nationwide Voluntary Recalls of Specific Lots of Five Generic Products Due to the Potential for Oversized Tablets Propafenone HCl Tablets 11/10/2008
MedWatch: FDA Reports Nationwide Recall of Mislabeled ReliOn Insulin Syringes 11/6/2008
MedWatch: Class 1 Recall: VIBE Technologies, Vibrational Integrated Bio-photonic Energizer (VIBE) Machine Multi-Frequency Field Generator 11/3/2008
MedWatch: Safety Labeling Changes Approved By FDA Center for Drug Evaluation and Research 11/3/2008
MedWatch: Thoratec Corporation (THOR) Issues Worldwide Medical Device Correction of HeartMate II(R) Left Ventricular Assist System 10/28/2008
MedWatch: FDA Approves Updated Labeling for Psoriasis Drug Raptiva 10/21/2008
MedWatch: FDA, ETHEX Corporation (KVa) Announce Dextroamphetamine Sulfate 5mg Tablets Update 10/16/2008
MedWatch: FDA Issues Notification About Over The Counter Cough and Cold Medications 10/13/2008
MedWatch: Tiotropium (marketed as Spiriva HandiHaler) Update 10/8/2008
MedWatch: Nebion, LLC HLX-8 Magnetic Resonance Device Recalled 10/6/2008
MedWatch: Medtronic, Inc. (MDT) Neuromodulation INDURA One-Piece Intrathecal Catheters 10/2/2008
MedWatch: FDA Analysis Shows Cholesterol Lowering Medications Do Not Increase the Risk of Lou Gehrig's Disease 9/30/2008
MedWatch: Preliminary Safety Findings Show More Deaths In Patients Given Epoetin-alpha Versus Placebo 9/26/2008
Genentech, Inc. (DNA) (JOBS), OSI Pharmaceuticals, Inc. (OSIP) Warn Of Liver Damage From Tarceva, 2 Deaths 9/24/2008
MedWatch: Ucyclyd Pharma, Inc. Announces Safety Update on Ammonul Injection Product 9/23/2008
Medwatch: Phosphocol P 32 - Risk of Leukemia Associated with Off-label Intra-Articular Use in Children 9/18/2008
MedWatch: August 2008 Safety-Related Labeling Changes 9/16/2008
MedWatch: Infant Formula Manufactured in China 9/12/2008
MedWatch: Rituxan Warning Label Update 9/11/2008
MedWatch: Class I Medical Device Recall: FDA LifePak CR Plus Automated External Defibrillators 9/11/2008
MedWatch: Disposable Battery Operated Lavage System Update 9/8/2008
MedWatch: Tumor Necrosis Factor-alpha Blockers, Cimzia, Enbrel, Humira, and Remicade Update 9/4/2008
MedWatch: September 2008 Patient Safety News 9/2/2008
MedWatch: FDA and Pacific Consolidated Industries, LLC Announce Class I Recall of Mobile Oxygen Storage Tank 8/28/2008
MedWatch: Two New Cases of Progressive Multifocal Leukoencephalopathy in European Patients Receiving Tysabri as Monotherapy for Multiple Sclerosis for More Than One Year 8/25/2008
MedWatch: FDA Has Received Reports of 6 Cases of Hemorrhagic or Necrotizing Pancreatitis in Patients in Taking Byetta Since October 2007 8/18/2008
MedWatch: July 2008 Safety-Related Labeling Changes 8/14/2008
MedWatch: Boston Scientific Corporation (BSX) NexStent Monorail, NexStent Carotid Stent and Monorail Delivery System Product Recalled 8/14/2008
MedWatch: Vivitrol Serious Injection Site Reactions May Occur with the use of Injectable Naltrexone 8/12/2008
MedWatch: Watson Pharmaceuticals, Inc. (WPI) Voluntarily Recalls Fentanyl Transdermal System CII Patches 8/12/2008
MedWatch: Simvastatin Used With Amiodarone Update 8/8/2008
MedWatch: Erythropoiesis Stimulating Agents Update 8/8/2008
MedWatch: Desmopressin Acetate Update 8/7/2008
Actavis Totowa Announces Voluntary Recall at the Retail Level of All Drug Products Manufactured at its Little Falls, New Jersey Facility 8/4/2008
MedWatch: EG Labs, LLC Recalls Viapro 375mg Capsules 7/31/2008
MedWatch: Jack Distribution, LLC's Rize 2 The Occasion, Rose 4 Her Capsules Recalled 7/31/2008
MedWatch: Amgen (AMGN), FDA Modify Boxed Warning of Erythropoiesis Stimulating Agents 7/31/2008
MedWatch: Mitoxantrone Hydrochloride Update 7/30/2008
MedWatch: June 2008 Safety Related Labeling Changes 7/30/2008
Medwatch: Abacavir (marketed as Ziagen) and Abacavir-containing Medications 7/24/2008
Medwatch: Micro-bubble Contrast Agents (marketed as Definity (Perflutren Lipid Microsphere) Injectable Suspension and Optison (Perflutren Protein-Type A Microspheres for Injection) 7/17/2008
Medwatch: Sodium Polystyrene Sulfonate Suspension 7/16/2008