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DRUGS AND MEDICINES 0 - 49 of 969 recalls/alerts 10/11/2005 FDA Alerts Physicians on Menactra Link to Guillain Barre Syndrome 10/11/2005 FDA Alerts Physicians on Menactra Link to Guillain Barre Syndrome 9/26/2005 FDA Alerts Healthcare Professionals on Changes to the Warnings for Erbitux 9/26/2005 FDA Alerts Healthcare Professionals on use of Herceptin 9/26/2005 FDA Issues Recall on BioMerieux VeriCal Callibrator Set 9/26/2005 FDA Recalls Injectable Products made by Central Admixture Pharmacy Service (CAPS) 9/26/2005 FDA, AstraZeneca Alerts Physicians on Toprol-XL 9/26/2005 Guidant Initiates Voluntary Physician Advisory on Certain Pacemakers 9/22/2005 Custom-Rx Compounding Pharmacy Issues Nationwide Recall of Trypan Blue 0.06% Ophthalmic Solution 8/19/2005 Gambro Dasco S.P.A. Issues Worldwide Safety Alert for the Prisma® System Renal Replacement System 8/17/2005 Guidant Corporation Recalls Pacemakers 8/17/2005 FDA Issues Safety Alert on Metallic Tracheal Stents 8/1/2005 Perrigo Company Announces Nationwide Recall of Infants' Oral Drops Containing Enclosed Syringe 7/29/2005 Disetronic Medical Systems, Inc. Recalls the D-TRON Adapters, Used With the D-TRONplus Insulin Pump 7/26/2005 FDA Announces Guidant's Class I Pacemaker Recall 7/26/2005 FDA Announces Class I Recall of Baxter Healthcare's Colleague Volumetric Infusion Pumps 7/19/2005 FDA Asks Purdue Pharma to Withdraw Palladone for Safety Reasons 7/19/2005 Guidant Initiates Worldwide Physician Communications Regarding Important Safety Information and Corrective Action about Certain Pacemakers 7/7/2005 FDA Updates Consumers on Guidant Corporation's Implantable Defibrillators 7/7/2005 FDA Issues Nationwide Alert for "Liqiang 4" Due to Potential Health Risk 7/5/2005 FDA Notified Consumers and Healthcare Professionals About The Risks of Taking Liqiang 4 Dietary Supplement Capsules 6/30/2005 FDA Issues Nationwide Notification of Recall of Certain Guidant Implantable Defibrillators and Cardiac Resynchronization Therapy Defibrillators 6/30/2005 W. Enterprises Expands its Nationwide Recall of Pet Treats to Include All of its Products Due to Possible Salmonella Contamination 6/30/2005 Bioniche Issues Recall of BetacTM 6/30/2005 Guidant Initiates Worldwide Physician Communications Regarding Important Safety Information and Corrective Action about Implantable Cardiac Defibrillators 6/30/2005 Boston Scientific Announces Worldwide Recall of Hemashield® Vantage Peripheral Vascular Grafts 6/23/2005 Guidant Implantable Defibrillator Recall Due to Inability to Deliver an Electrical Shock During Episodes of Arrhythmia 6/16/2005 Quality Care Products L.L.C. Able Laboratories Inc. Nationwide Recall 6/16/2005 Murry's, Inc. Recalls 63,850 Pounds of Frozen Ground Beef Products 6/16/2005 McNeil Consumer & Specialty Pharmaceuticals Announces Nationwide Recall of Children's Tylenol Meltaways - 80 Mg, Children's Tylenol Softchews - 80 Mg and Jr. Tylenol Meltaways - 160 Mg 6/16/2005 Qualitest Pharmaceuticals, Inc. Issues a Voluntary Nationwide Recall of Accusure Insulin Syringes 1cc 28 Gauge 1/2 Inch 100's 5/31/2005 FDA Advises Consumers about Recalled Drugs from Able Laboratories 5/26/2005 The Master's Miracle Issues Nationwide Health Alert Against Applying Their Products to the Eyes 5/26/2005 Biomerieux Issues New Alert on the Recall of Certain Lots of Its Simplastin Tissue Reagent Used in Laboratory Monitoring of Oral Anticoagulant Therapy 5/12/2005 MRL, Inc. a Welch Allyn Company Issues a Voluntary Worldwide Recall of Selected AED20 Automatic External Defibrillators 5/10/2005 MRI-Caused Injuries in Patients with Implanted Neurological Stimulators 5/3/2005 Pfizer Follows Up On February, 2005 Recall of One Lot Of Epilepsy Medicine 5/3/2005 Medtronic Announces Additional Devices Affected in Voluntary Recall of Certain Monophasic LifePak ® 500 Automated External Defibrillators 5/3/2005 Kingswood Laboratories, Inc. Issues Nationwide Recall of Moi-Stir Oral Swabsticks 5/3/2005 Bedford Laboratories Recalls One Lot of Famotidine Injection 5/3/2005 Laerdal Medical Announces Voluntary Nationwide Recall of Adapter Cable for Certain Defibrillators 5/3/2005 Amerisource Health Services Recalls One Lot of Famotadine Injection 4/12/2005 PharMEDium Services Initiates Nationwide Magnesium Sulfate Solution Recall of All 50 ml Admixtures of MgSO4 in 5% Dextrose Because of a Potential Lack of Sterility Assurance 4/7/2005 FDA Requests That Pfizer, Inc. Voluntarily Recall Bextra (Valdecoxib) From The Market 4/4/2005 Dade Behring has Voluntarily Issued Nationwide Recall Of Microscan® Rapid Pos Inoculum Broth 3/28/2005 Nationwide Alert On B-Sure Pregnancy Test 3/21/2005 Elanco Animal Health Issues Recall of Lot Number 43650A of Micotil® 300 (tilmicosin injection) 3/21/2005 Heartsine Technologies, Inc. Issues Worldwide Recall of Certain Automatic External Defibrillators 3/10/2005 FDA Medwatch - Public Health Advisory Issued For Elidel ( Pimecro Limus) And Protopic (Tacrolimus) 3/8/2005 FDA MedWatch - U.S. Marshals seized lots of GlaxoSmithKline's Pax il CR (paroxetine hydrochloride) and Avandamet (rosiglitazone maleate + m etformin hydrochloride)   next >> Automotive Child Safety Drugs & Medicines Food Allergies Food Contamination Home & Electronic Outdoors How Recalls Work LINKS OF INTEREST Recent Lawsuits Marketing@Law Websites@Law ClassActionAmerica USJuris KGLG Class Action Vioxx Lawyer Attorneys Bextra Lawyer Recalls SEARCH WITH The Web This Site   Need Lawyer Help Make a Complaint

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