FDA Proposes Rule on Unsafe Device Removal Reporting
CMBE & SBET Recommend Cellular Phone Ban & RFI Standards Review
Pulse Generators may Show Unintentional Safety Reversion Mode
Disposable I.V. Administration Sets Packaged With Wrong Tubing
Anesthetic Gas Monitors may Display Wrong Agent
Drug Infusion Pump Data may Conflict With Package Insert Protocols
Endoscopie Ligator Overtubes Lack 510(k)
Blood Tubing may Disconnect From Dialyzer Luer Connection
Irrigation System Recall due to Flow Blockage
Electrophysiology Catheter Recall Complete
Intra-Aortic Balloon Pumps Recalled Because of Power Board Failures
Coronary Balloon Catheters Incorrectly Labeled
Ventilator Control Valve Recall Complete
Comments Sought on Standards for Biological Evaluation of Medical Devices
Revisions Proposed for Vascular Graft Prostheses Standard
Judge Sets Filing Deadlines in $5.2-Billion Breast Implant Settlement
Spirometry Filters to Provide Device Cross-Contamination Barrier
Cellular Phones
AIHA Conference & Exposition