{"id":7069,"date":"2013-11-15T21:31:19","date_gmt":"2013-11-16T05:31:19","guid":{"rendered":"http:\/\/www.foodanddrugrecall.org\/index.php\/fda-classifies-medtronics-worldwide-voluntary-field-action-on-guidewires-as-class-i-recall\/"},"modified":"2013-11-15T21:31:19","modified_gmt":"2013-11-16T05:31:19","slug":"fda-classifies-medtronics-worldwide-voluntary-field-action-on-guidewires-as-class-i-recall","status":"publish","type":"post","link":"https:\/\/www.foodanddrugrecall.org\/index.php\/fda-classifies-medtronics-worldwide-voluntary-field-action-on-guidewires-as-class-i-recall\/","title":{"rendered":"FDA Classifies Medtronic&#8217;s Worldwide Voluntary Field Action on Guidewires as Class I Recall"},"content":{"rendered":"<p>Medtronic, Inc. (NYSE: MDT) announced today that the U.S. Food and Drug Administration (FDA) has classified the company&#8217;s recently initiated voluntary field action related to certain guidewires as a Class I recall.<br \/>\nBased on an internal investigation following a limited number of complaints, including one patient injury, Medtronic began notifying hospitals and distributors worldwide the week of Oct. 21 that some models of its guidewires from recent lots have the potential for the coating on their surface to delaminate and detach.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Medtronic, Inc. (NYSE: MDT) announced today that the U.S. Food and Drug Administration (FDA) has classified the company&#8217;s recently initiated voluntary field action related to certain guidewires as a Class I recall. Based on an internal investigation following a limited number of complaints, including one patient injury, Medtronic began notifying hospitals and distributors worldwide the &hellip; <a href=\"https:\/\/www.foodanddrugrecall.org\/index.php\/fda-classifies-medtronics-worldwide-voluntary-field-action-on-guidewires-as-class-i-recall\/\" class=\"more-link\">Continue reading <span class=\"screen-reader-text\">FDA Classifies Medtronic&#8217;s Worldwide Voluntary Field Action on Guidewires as Class I Recall<\/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-7069","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\/7069","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=7069"}],"version-history":[{"count":0,"href":"https:\/\/www.foodanddrugrecall.org\/index.php\/wp-json\/wp\/v2\/posts\/7069\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.foodanddrugrecall.org\/index.php\/wp-json\/wp\/v2\/media?parent=7069"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.foodanddrugrecall.org\/index.php\/wp-json\/wp\/v2\/categories?post=7069"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.foodanddrugrecall.org\/index.php\/wp-json\/wp\/v2\/tags?post=7069"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}