FDA Slow to Implement Mandotory Reporting
Polyurethane Pacemaker Leads Subject to Safety Alert
Scheostomy Sets Withdrawn From market in Canda But Not in U.S
Residual Aldehyde Detector Recalled Because of Iron Contamination
FDA Reports Recall Completed Two Years Ago
Antiseptic Causes Cracks in Catheter Hubs
International Manufacturing QA & Sterilization Standards Under Revery
Laparotomy Sponge “Unintential plants” Often Lead to Lawsuits
OSHA Imposes Fines on Hospital
FDA Warns of Possible Patient Restraint Hazards
Sithotripter Shock-Wave Measurement Guidance Available
Radiographic QA Testing System