{"id":8810,"date":"2016-01-27T11:48:00","date_gmt":"2016-01-27T19:48:00","guid":{"rendered":"http:\/\/www.foodanddrugrecall.org\/index.php\/fda-classifies-st-jude-medical-field-action-for-447-of-the-companys-optisure-high-voltage-leads-as-a-class-1-advisory-in-the-u-s\/"},"modified":"2016-01-27T11:48:00","modified_gmt":"2016-01-27T19:48:00","slug":"fda-classifies-st-jude-medical-field-action-for-447-of-the-companys-optisure-high-voltage-leads-as-a-class-1-advisory-in-the-u-s","status":"publish","type":"post","link":"https:\/\/www.foodanddrugrecall.org\/index.php\/fda-classifies-st-jude-medical-field-action-for-447-of-the-companys-optisure-high-voltage-leads-as-a-class-1-advisory-in-the-u-s\/","title":{"rendered":"FDA Classifies St. Jude Medical Field Action For 447 Of The Company\u2019s Optisure High Voltage Leads As A Class 1 Advisory In The U.S."},"content":{"rendered":"<p>St. Jude Medical, Inc. (NYSE:STJ), a global medical device company, today announced that a previously communicated voluntary global field safety action related to the company\u2019s Optisure\u2122 Dual Coil Defibrillation Leads has now been classified as a Class 1 Advisory by the U.S. Food and Drug Administration. The Class 1 Advisory relates to a limited and well-defined group of 447 Optisure leads, 278 of which were distributed in the U.S., which may have been damaged during a manufacturing step.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>St. Jude Medical, Inc. (NYSE:STJ), a global medical device company, today announced that a previously communicated voluntary global field safety action related to the company\u2019s Optisure\u2122 Dual Coil Defibrillation Leads has now been classified as a Class 1 Advisory by the U.S. Food and Drug Administration. The Class 1 Advisory relates to a limited and &hellip; <a href=\"https:\/\/www.foodanddrugrecall.org\/index.php\/fda-classifies-st-jude-medical-field-action-for-447-of-the-companys-optisure-high-voltage-leads-as-a-class-1-advisory-in-the-u-s\/\" class=\"more-link\">Continue reading <span class=\"screen-reader-text\">FDA Classifies St. Jude Medical Field Action For 447 Of The Company\u2019s Optisure High Voltage Leads As A Class 1 Advisory In The U.S.<\/span> <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"1","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[3],"tags":[],"class_list":["post-8810","post","type-post","status-publish","format-standard","hentry","category-food-drug-recalls"],"_links":{"self":[{"href":"https:\/\/www.foodanddrugrecall.org\/index.php\/wp-json\/wp\/v2\/posts\/8810","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.foodanddrugrecall.org\/index.php\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.foodanddrugrecall.org\/index.php\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.foodanddrugrecall.org\/index.php\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.foodanddrugrecall.org\/index.php\/wp-json\/wp\/v2\/comments?post=8810"}],"version-history":[{"count":0,"href":"https:\/\/www.foodanddrugrecall.org\/index.php\/wp-json\/wp\/v2\/posts\/8810\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.foodanddrugrecall.org\/index.php\/wp-json\/wp\/v2\/media?parent=8810"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.foodanddrugrecall.org\/index.php\/wp-json\/wp\/v2\/categories?post=8810"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.foodanddrugrecall.org\/index.php\/wp-json\/wp\/v2\/tags?post=8810"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}