User Reporting Rules Draw Fire From Hospitals & Industry
Dialysis Patient Bleeds to Death From Needle Dislodgement
“Mandatory Recall” of Sterilizing Solution Under Safe Devices Law
Possible “No Output” Condition From Pacemaker Capacitor Failure
Possible Burn Hazard From Transilluminator Filter Assemblies
Oxygenator Recall Classified
Fragmentation Needles Could Break Off From Hub
Device-Punctured Packaging Leads to Recall of Retraction Clips
Pacemaker Lead Shelf-Life Information Incorrect
Faulty High-Temperature Switches Alleged in Patient Burn Death
FDA Answers Questions on User Reporting
Biomedical Equipment Technician Sought
Quest Publishing to Exhibit at AAMI Meeting