Coma Caused When MRI is Performed on Patient with Implanted Neurological Stimulator
More Class I Recalls Involving AEDs
Class I Recall
Advanced D-Dimer Assay Recalled
Stem Adapters Recalled; Risk of Separation Cited
Tibial Insert Recall Complete
Rapid Syphilis Test Kits Recalled
Bone Tap Instrument Subject Of Recall
Uncontrolled Table Motion Prompts Recall of CT Device
Defective Units Lead to Recall of Generator
CT Injector System Part Recalled; Fall Possible
Neonatal/Infant Breathing Circuits Recalled
Sterility Concern Leads to Recall of Embolectomy Catheters
Dissecting Sealer Recalled; Tip May Separate
Release of Pressure Prompts Cuff Recall
Insulin Cartridges Recalled; Leakage Reported
FDA Approves Genetic Test For Cystic Fibrosis
New Details on Hospital Bed Seizure
First Sealant for Dura Mater Approved by FDA
New Arrhythmia Ablation System Approved