{"id":22217,"date":"2013-01-31T18:46:14","date_gmt":"2013-01-31T23:46:14","guid":{"rendered":"http:\/\/www.gblawyers.com\/?p=22217"},"modified":"2015-07-14T11:23:32","modified_gmt":"2015-07-14T15:23:32","slug":"depuy-executive-asked-why-plans-to-re-design-asr-hip-halted","status":"publish","type":"post","link":"https:\/\/www.gblawyers.com\/blog\/depuy-executive-asked-why-plans-to-re-design-asr-hip-halted\/","title":{"rendered":"DePuy Executive Asked Why Plans to Re-Design ASR Hip Halted"},"content":{"rendered":"<p>The president of the orthopedic division of Johnson &amp; Johnson, Andrew Ekdahl, said the company recalled their all-metal implant due to it not meeting &#8220;clinical needs for the product.&#8221; He testified at a trial recently due to claims the company failed to issue warnings about the risks involved with the implants. He was questioned by a representative for a patient adversely affected by their hip implant about whether they recalled the implants because they were not safe, but he continued to answer that they did not meet clinical needs.<\/p>\n<p>In 2010, the company said 12% of devices failed.\u00a0 By 2011, a study showed 37% failed, and in 2012 44% were found to fail within seven years. Ekdahl was asked how many hip revision surgeries due to failure were expected, and what they considered acceptable. He said they didn&#8217;t know the acceptable rate.<\/p>\n<p>He was also asked about their handling of complaints filed by surgeons because thousands stated the device caused them painful symptoms. A surgeon stated the hips were poorly designed. Ekdahl was also questioned about their plans to re-design the implant that were scrapped, according to <a href=\"http:\/\/www.bloomberg.com\/news\/2013-01-30\/j-j-s-ekdahl-says-hips-recalled-because-of-clinical-needs.html\" target=\"_blank\">news reports<\/a>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>The president of the orthopedic division of Johnson &amp; Johnson, Andrew Ekdahl, said the company recalled their all-metal implant due to it not meeting &#8220;clinical needs for the product.&#8221; He testified at a trial recently due to claims the company failed to issue warnings about the risks involved with the implants. He was questioned by [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[4],"tags":[],"class_list":["post-22217","post","type-post","status-publish","format-standard","hentry","category-defective-medical-devices"],"_links":{"self":[{"href":"https:\/\/www.gblawyers.com\/blog\/wp-json\/wp\/v2\/posts\/22217","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.gblawyers.com\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.gblawyers.com\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.gblawyers.com\/blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.gblawyers.com\/blog\/wp-json\/wp\/v2\/comments?post=22217"}],"version-history":[{"count":1,"href":"https:\/\/www.gblawyers.com\/blog\/wp-json\/wp\/v2\/posts\/22217\/revisions"}],"predecessor-version":[{"id":23351,"href":"https:\/\/www.gblawyers.com\/blog\/wp-json\/wp\/v2\/posts\/22217\/revisions\/23351"}],"wp:attachment":[{"href":"https:\/\/www.gblawyers.com\/blog\/wp-json\/wp\/v2\/media?parent=22217"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.gblawyers.com\/blog\/wp-json\/wp\/v2\/categories?post=22217"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.gblawyers.com\/blog\/wp-json\/wp\/v2\/tags?post=22217"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}