FDA Warns of Possible Spinal Anesthesia Injury
FDA Finds Improper Restraint Device Use Kills Over 100 Patients Per Year
Rotary Atherectomy Catheters Recalled After Device Failures
Air in Dialysis Lines May Reach Patient
Outdated Recall Leads to Hemoperfusion Cartridge Safety Alert
3M Withdraws From Glutaraldehyde Disinfectant Market
High-Frequency Ventilation Theory Videotape Recalled
ECG Electrodes Did Not Meet Noise & Artifact Specifications
Laser Beam Attenuators Could Allow Access to Radiation
Specification Problems For Cochlear Implants
Laparoscopic Suction Spatula Can Shock User
Co2 Cartridge Holders Redesigned to Prevent Gas Pressure Hazard
$6.5 Million Ventilator-Related Brain-Injury Award Upheld
Disinfectant Claims Issue Settled & FDA Clearance Granted