ProfessionalsInformation for Professionals
Special Alert Archive
- Coumadin 1 mg Tablet Blister Packs: Recall - 07/14/10
- Qualaquin (quinine sulfate): New Risk Management Plan due to potential for serious hematological reactions - 07/08/10
- FDA - LIFEPAK 20 and LIFEPAK 20e External Defibrillator/Monitors by Physio-Control Inc.: Class I Recall Due To Power Supply Failure -07/02/10
- FDA: Tamiflu: Counterfeit Product Sold on Internet - risk for those allergic to penicillins - 06/17/10
- FDA Recall of Defibtech DBP-2800 Battery Packs used in Lifeline AED and ReviveR AED - 06/14/10
- FDA Public Health Alert: Healthcare Professionals Warned Not To Use Certain Intravenous Metronidazole, Ondansetron, and Ciprofloxacin Due To Potential Contamination - 05/31/10
- Unomedical Issues Worldwide Recall of Certain Manual Pulmonary Resuscitators - 10/12/09
- Recall of LIFEPAK CR Plus Automated External Defibrillators (Physio-Control, Inc) - 09/10/09
- Myfortic (mycophenolic acid) - 09/08/09
- Accusure Insulin Syringes [31G, 1/2 cc and 1 cc] - 08/24/09
- FDA Public Health Notification: Potentially Fatal Errors with GDH-PQQ* Glucose Monitoring Technology - 08/13/09
- Serious Errors with Certain Blood Glucose Monitoring Test Strips (GDH-PDQ) – For Diabetic patients and/or their caregivers - 08/13/09
- Notice to Dietitians from the Texas State Board of Examiners - 07/02/09
- CMS Response to Drawing Normal Saline at the Chair Side - 07/02/09
- FEMA 211 Registration - 06/01/09
- Hepatitis B Vaccine Shortage - 06/01/09
- Recall of ZOLL AED Plus Defibrillator - 04/09/09
- Updated
Position Statement for NxStage PureFlow and NxStage System One Home
Dialysis
Products - 04/09/09 - Caraco Pharmaceutical Laboratories, Ltd. Announces a Nationwide Voluntary Recall of All Lots of Digoxin Tablets Due to Size Variability - 04/01/09
- Peanut Recall - up-to-date information and listings from the FDA
- Recall of Mislabeled ReliOn Insulin Syringes - 11/11/08
- Class 1 Recall: Physio Control, Inc. LifePak CR Plus Automated External Defibrillators (AEDs) - 09/11/08
- Morton Salt Additive - FDA Determination - 08/21/08
- FDA Alert - Sodium Polystyrene Sulfonate Suspension (Kayexalate) - 07/21/08
- Morton Salt for Water Treatment Alert - 07/03/08
- FDA Heparin Recall - 06/13/08
- Revised Position Statement for NxStage PureFlow and NxStage System One Home Dialysis Products - 03/26/08
- “Tamper Resistant” Prescription Requirement - 03/25/08
- FDA MedWatch Notice re: Baxter Heparin Recall - 02/29/08
- Position Statement for NxStage PureFlow and NxStage System One Home Dialysis Products - 01/25/08
- FDA Warnings and Instructions for Heparin Sodium Injection Use - 02/12/08
- Recall of Baxter Heparin - 01/21/08
- State of Texas Facts
- Notice of Legislative Change for EMS providers
- Vinegar Use in Hemodialysis
- MRB Recommendations on Use of Non-Standard Baths
- KHC Medicare Part D Coordination of Benefits for 2008
- Carbon Monoxide Alert Memo
- Carbon Monoxide Fact sheet