{"id":6414,"date":"2017-04-07T09:51:30","date_gmt":"2017-04-07T13:51:30","guid":{"rendered":"https:\/\/medicarereport.org\/?p=6414"},"modified":"2017-04-07T09:51:30","modified_gmt":"2017-04-07T13:51:30","slug":"recall-alert-medical-device","status":"publish","type":"post","link":"https:\/\/medicarereport.org\/?p=6414","title":{"rendered":"Recall Alert:  Medical Device"},"content":{"rendered":"<p><span style=\"margin: 0px; color: #111111; font-family: 'Calibri','sans-serif';\">On Thursday, Medtronic Plc said it was <\/span><span style=\"margin: 0px; color: #111111; font-family: 'Calibri','sans-serif';\">conducting the voluntary recall due to an issue that can occur after implantation, potentially leading to under-drainage of cerebrospinal fluid.<\/span><span style=\"color: #000000; font-family: Times New Roman;\"> <a href=\"http:\/\/www.reuters.com\/article\/us-medtronic-recall-idUSKBN1782VZ\" target=\"_blank\">Read article here\u2026<\/a><\/span><\/p>\n<pre style=\"border: 1px solid #eaeaea; font-variant-ligatures: normal; font-variant-caps: normal; font-variant-numeric: inherit; font-stretch: inherit; line-height: 1.4; font-family: 'Courier 10 Pitch', Courier, monospace; font-size: 14px; font-style: normal; font-weight: normal; margin: 0px 0px 20px; outline: 0px; padding: 20px; vertical-align: baseline; background-color: #ffffff; overflow: auto; white-space: pre-wrap; color: #444444; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; text-decoration-style: initial; text-decoration-color: initial;\"><strong>Notice<\/strong>: The link provided above connects readers to the full content of the posted article. The URL (internet address) for this link is valid on the posted date; medicarereport.org cannot guarantee the duration of the link\u2019s validity. Also, the opinions expressed in these postings are the viewpoints of the original source and are not explicitly endorsed by AMAC, Inc.; the AMAC Foundation, Inc.; or medicarereport.org.<\/pre>\n","protected":false},"excerpt":{"rendered":"<p>On Thursday, Medtronic Plc said it was conducting the voluntary recall due to an issue that can occur after implantation,<\/p>\n","protected":false},"author":5,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[14],"tags":[],"class_list":["post-6414","post","type-post","status-publish","format-standard","hentry","category-medical-technology"],"_links":{"self":[{"href":"https:\/\/medicarereport.org\/index.php?rest_route=\/wp\/v2\/posts\/6414","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/medicarereport.org\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/medicarereport.org\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/medicarereport.org\/index.php?rest_route=\/wp\/v2\/users\/5"}],"replies":[{"embeddable":true,"href":"https:\/\/medicarereport.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=6414"}],"version-history":[{"count":1,"href":"https:\/\/medicarereport.org\/index.php?rest_route=\/wp\/v2\/posts\/6414\/revisions"}],"predecessor-version":[{"id":6415,"href":"https:\/\/medicarereport.org\/index.php?rest_route=\/wp\/v2\/posts\/6414\/revisions\/6415"}],"wp:attachment":[{"href":"https:\/\/medicarereport.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=6414"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/medicarereport.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=6414"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/medicarereport.org\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=6414"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}