More Adverse Events With Guidant's Implantable Cardioverter Defibrillators
Volumetric Infusion Pumps Recalled
Defibrillators Recalled; Previous Recommendation Revised
Cracks, Peeling Lead to Recall of Introducer Sheaths
Recall of Central Venous Catheter Complete
Separation, Choking Hazard Prompt Recall of Adapter
PCA Syringe Pump Recalled; May Stop Infusion
Lack of Shutdown Alarm Leads to Ventilator Recall
Motorized Vehicles Recalled; Loose Screw Possible
Laser System Recalled; Software Anomaly Cited
Incorrect Reporting Prompts Recall of Diagnostic Software
Recall of Tibial Tray Complete
Blood Filtration System Recalled Due to Self-Test Problem
Shock Hazard Prompts Recall of Equipment
Hemodialysis Systems Recalled for Manual Addenda
Aortic Cutter Subject of Recall
Corrupted Data Prompts Imaging System Recall
Lightweight Cassettes Recalled; Unsatisfactory Sharpness Noted
Disinfectant Spray Fails EPA Testing; Recall Begun
Nonsterile Cataract Surgeries In China