St. Jude Medical Recalls Defibrillator Leads Due to Damaged Insulation
On January 22, 2016, device maker St. Jude Medical announced that a voluntary global field safety action related for the company's Optisure Dual Coil Defibrillation Leads has now been designated a Class 1 advisory by the Food and Drug Administration (FDA). Damaged leads may lead to an electrical malfunction wherein the defibrillator … [Read more...] about St. Jude Medical Recalls Defibrillator Leads Due to Damaged Insulation
Medtronic Announces Voluntary Recall of of Older ICD Models
Two older models of implantable cardioverter defibrillator recalled.Medtronic, Inc. announced that it is voluntarily recalling two older models of implantable cardioverter defibrillator due to a defect. The Class I recall involves a small subset of Micro Jewel® II Model 7223Cx and GEM® DR Model 7271 ICDs. this two devices may … [Read more...] about Medtronic Announces Voluntary Recall of of Older ICD Models
