FDA Defibrillator Use Recommendations Questioned
Healthcare Workers Advised to Control N2O Exposure
FDA Reissues Safety Alert on TMJ Implant Problems
Plunger-Type Resuscitators Recalled After FDA Halts Clinical Trials
EEG Cable Labeling Fails to Contraindicate Apnea Monitor Use
Cracked Luer Lock Could Cause Improper Infusion
Blood Warmers Could Shock if Loose Wires Contact EMI Shield
Temperature-Sensitive Pacing Circuit Could Activate Before Enabled
Weak Packaging Seals Compromise Sterility on Infusion Sets & Bags
Biotronik Disputes “Recall” of Implantable Pulse Generator
Tympanic Thermometers Inadequately Shielded From EMI
Adoption of ISO Draft Sterilization & Cardiac Implant Standards Proposed
ER Doctor Disabled by “Mystery Fumes” Files $6-Million Claim
GAO Asked to Identify Scope of EMI-Related Device Malfunction
First EMC Challenge Forum