FDA to Remove “Essential Use” Exemption For CFCs in Epinephrine Inhalers
Class I Recall : Automatic External Defibrillator
Patient Information Software Recalled
6 Million Drug Transfer Devices Recalled
Contaminated Culture Bottles Recalled
Potential Shock Hazard Leads To Steam Sterilizer Recall
Blood Gas Analyzer Recalled; Waste Fluid May Escape
Imaging Accessory Recalled; Positioning Errors Possible
Hematology Analyzer Recalled
Surgical Kits Recalled for Sterility Problems
Coronary Stent System Recalled
Recall of 1.8 Million Cassette Reservoirs
Swivel Collimators Recalled
33 Million Test Strips Recalled
Faulty Software Recalled
Acid Fumes Prompt Anesthesia Workstation Recall
Surgical Gloves Recalled
Johnson & Johnson Loses Latest Round in Stent Battle : Cites Poor Performance of Own Device in Patent Infringement Defense