FDA Estimates on Device Reports Miss the Mark
Modified Dialyzer Reprocessing Eliminates Acute Allergic Reactions
Premature Battery Depletion in Pacemakers Leads to Canadian Device-Incident Monitoring
Bag Resuscitators Recalled Because of Dislodged Valves
Electrosurgical Pencil Switches May Have Been Deformed by EtO Sterilization
Additional Surgical Instrument Trays Affected by EtO Residue
Pressure Relief Valve Leakage Problem Resulted from Stress Cracks
Pacemaker Battery Problems Continue : Recall & Extension of Serial Numbers
Infusion-Line Regulator May Allow Fluid Seepage
Automated External Defibrillator Initiative Calls for Early Action
Directory of Hospital Personnel Published
Should Biomedical Engineers Advise on Healthcare Policy?
Testing Laboratory & Inspection Agency Accreditation Standards