{"id":4823,"date":"2012-06-19T10:04:12","date_gmt":"2012-06-19T18:04:12","guid":{"rendered":"http:\/\/www.foodanddrugrecall.org\/index.php\/nidek-medical-products-inc-issues-an-urgent-medical-device-correction-affecting-oxygen-concentrators\/"},"modified":"2012-06-19T10:04:12","modified_gmt":"2012-06-19T18:04:12","slug":"nidek-medical-products-inc-issues-an-urgent-medical-device-correction-affecting-oxygen-concentrators","status":"publish","type":"post","link":"https:\/\/www.foodanddrugrecall.org\/index.php\/nidek-medical-products-inc-issues-an-urgent-medical-device-correction-affecting-oxygen-concentrators\/","title":{"rendered":"Nidek Medical Products, Inc. issues an Urgent Medical Device Correction affecting oxygen concentrators"},"content":{"rendered":"<p>Nidek Medical Products, Inc., today announced that the U.S. Food and Drug Administration (FDA) has classified Nidek\u2019s voluntary recall action regarding capacitor-related fires in Medical Mark5 Nuvo Lite Oxygen concentrators as a Class I recall. The affected devices were manufactured and distributed from January 2004 through May 2010 with serial numbers in the range of 042-10000 through 102-09335.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Nidek Medical Products, Inc., today announced that the U.S. Food and Drug Administration (FDA) has classified Nidek\u2019s voluntary recall action regarding capacitor-related fires in Medical Mark5 Nuvo Lite Oxygen concentrators as a Class I recall. The affected devices were manufactured and distributed from January 2004 through May 2010 with serial numbers in the range of &hellip; <a href=\"https:\/\/www.foodanddrugrecall.org\/index.php\/nidek-medical-products-inc-issues-an-urgent-medical-device-correction-affecting-oxygen-concentrators\/\" class=\"more-link\">Continue reading <span class=\"screen-reader-text\">Nidek Medical Products, Inc. issues an Urgent Medical Device Correction affecting oxygen concentrators<\/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-4823","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\/4823","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=4823"}],"version-history":[{"count":0,"href":"https:\/\/www.foodanddrugrecall.org\/index.php\/wp-json\/wp\/v2\/posts\/4823\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.foodanddrugrecall.org\/index.php\/wp-json\/wp\/v2\/media?parent=4823"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.foodanddrugrecall.org\/index.php\/wp-json\/wp\/v2\/categories?post=4823"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.foodanddrugrecall.org\/index.php\/wp-json\/wp\/v2\/tags?post=4823"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}