{"id":252,"date":"2016-11-28T14:34:48","date_gmt":"2016-11-28T14:34:48","guid":{"rendered":"https:\/\/www.groupactionlawyers.co.uk\/blog\/?p=252"},"modified":"2016-12-21T14:25:47","modified_gmt":"2016-12-21T14:25:47","slug":"implantable-cardioverter-defibrillators-batteries-causing-adverse-effect-atients","status":"publish","type":"post","link":"https:\/\/www.groupactionlawyers.co.uk\/blog\/implantable-cardioverter-defibrillators-batteries-causing-adverse-effect-atients","title":{"rendered":"&#8220;Medical device battery fault that have caused two deaths&#8221; &#8211; Battery defects of the implantable cardioverter defibrillators and cardiac resynchronisation therapy devices causing an adverse effect on patients"},"content":{"rendered":"<p>Due to a battery issue, medical equipment like implantable cardioverter defibrillators (ICD) and cardiac resynchronisation therapy devices (CRT-D) have reportedly failed, leading to serious concerns for patient health.<\/p>\n<p>It&#8217;s thought that around 350,000 devices worldwide have been implanted and potentially put patient health at risk.<br \/>\n<!--more--><\/p>\n<h2>Technical details<\/h2>\n<p>Lithium clusters forming from battery depletion can apparently bring about short circuiting, meaning the battery could drain very quickly. They&#8217;re supposed to last three months, but are possibly depleting quicker as a result of the problems, putting patient&#8217;s health &#8211; and lives &#8211; at risk.<\/p>\n<p>St Jude Medical published a notice to the public addressing the problem in the last few weeks, with the notice highlighting the affected models. The premature battery depletion associated with the devices manufactured by Fortify, Fortify Assura, Quadra Assura, Quadra Assura MP, Unify, Unify Assura and Unify Quada are said to be in the mix.<\/p>\n<h3>Consequences<\/h3>\n<p>There have been two deaths (one in the U.K.) that have been associated with the battery depletion. In those cases, the patients were unable to have their defibrillation therapy as a result of the devices draining out of battery prematurely.<\/p>\n<p>Additionally, there has been ten reported incidents of fainting as well.<\/p>\n<p>St Jude Medical reports that only 0.2% of the affected devices are reported to have experienced the premature battery depletion. Patients with devices implanted for a duration of more than six years have yet to be given any further information about any failure rates, which could put individuals at greater risk of harm.<\/p>\n<p><strong>Devices are reportedly being replaced at no extra cost.<\/strong><\/p>\n<p>As it seems impossible to predict which devices will suffer from the lithium cluster problem, the job of manufacturer is to recall all devices as soon as possible to have them rigorously tested for the issue. This is important given that it could be a life or death matter if devices fail.<\/p>\n<p>St Jude Medical&#8217;s plan of action so far only seeks to replace implanted devices that are nearly reaching its elective replacement indicator (ERI), which they see as the priority when it may be close to the end of life (EOL) of the device.<\/p>\n<h3>Large volumes affected<\/h3>\n<p>Although the distribution figure of 400,000 may seem nominal, it&#8217;s not as straight-forward as it seems.<\/p>\n<p>It&#8217;s not just NHS hospitals that are in recipient of the devices. The devices have been distributed among care homes, clinics, education colleges, hospices, independent treatment centres, nursing agencies and private medical practices.<\/p>\n<p>Which is huge.<\/p>\n<p>Acting on professional advice, St Jude Medical has given recommendations regarding the devices. However, they highlighted that individual patients may require individual considerations to be assessed on a case by case basis.<\/p>\n<p>St Jude Medical&#8217;s seemingly relaxed attitude in recalling all the affected devices could have harmful consequences for patients. A device that has the potential to cause death should be one that sees stringent prevention methods in place, and watchdogs scrutinising their every move.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Due to a battery issue, medical equipment like implantable cardioverter defibrillators (ICD) and cardiac resynchronisation therapy devices (CRT-D) have reportedly failed, leading to serious concerns for patient health. It&#8217;s thought that around 350,000 devices worldwide have been implanted and potentially put patient health at risk.<\/p>\n","protected":false},"author":1,"featured_media":255,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_jetpack_newsletter_access":"","_jetpack_dont_email_post_to_subs":false,"_jetpack_newsletter_tier_id":0,"_jetpack_memberships_contains_paywalled_content":false,"_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":false,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2},"jetpack_post_was_ever_published":false},"categories":[5],"tags":[],"class_list":["post-252","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-medical"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Implantable Cardioverter Defibrillators Batteries Causing Adverse Effect On Patients<\/title>\n<meta name=\"description\" content=\"It&#039;s thought that around 350,000 devices worldwide have been implanted and so far two deaths (one in the U.K.) associated to the depletion of the batteries.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.groupactionlawyers.co.uk\/blog\/implantable-cardioverter-defibrillators-batteries-causing-adverse-effect-atients\" \/>\n<meta property=\"og:locale\" content=\"en_GB\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Implantable Cardioverter Defibrillators Batteries Causing Adverse Effect On Patients\" \/>\n<meta property=\"og:description\" content=\"It&#039;s thought that around 350,000 devices worldwide have been implanted and so far two deaths (one in the U.K.) associated to the depletion of the batteries.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.groupactionlawyers.co.uk\/blog\/implantable-cardioverter-defibrillators-batteries-causing-adverse-effect-atients\" \/>\n<meta property=\"og:site_name\" content=\"Group Action Lawyers\" \/>\n<meta property=\"article:published_time\" content=\"2016-11-28T14:34:48+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2016-12-21T14:25:47+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/i1.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/11\/battery-implants-large.png?fit=725%2C544&ssl=1\" \/>\n\t<meta property=\"og:image:width\" content=\"725\" \/>\n\t<meta property=\"og:image:height\" content=\"544\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/png\" \/>\n<meta name=\"author\" content=\"Author\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:image\" content=\"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/11\/battery-implants-large.png?fit=725%2C544&ssl=1\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Author\" \/>\n\t<meta name=\"twitter:label2\" content=\"Estimated reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"2 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/www.groupactionlawyers.co.uk\\\/blog\\\/implantable-cardioverter-defibrillators-batteries-causing-adverse-effect-atients#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.groupactionlawyers.co.uk\\\/blog\\\/implantable-cardioverter-defibrillators-batteries-causing-adverse-effect-atients\"},\"author\":{\"name\":\"Author\",\"@id\":\"https:\\\/\\\/www.groupactionlawyers.co.uk\\\/blog\\\/#\\\/schema\\\/person\\\/0203ba576ea8f4e8ec318e9677b2a84b\"},\"headline\":\"&#8220;Medical device battery fault that have caused two deaths&#8221; 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The HeartStart MRx defibrillators are manufactured by Philips Healthcare and it's believed the fault lies with the batteries. 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It seems that medical device companies do not prioritise the safety of their products above profits and reputation, as a study conducted by the University of Minnesota revealed that these companies tend to delay in recalling defective products. When problems are not reported to relevant\u2026","rel":"","context":"In &quot;Medical&quot;","block_context":{"text":"Medical","link":"https:\/\/www.groupactionlawyers.co.uk\/blog\/category\/medical"},"img":{"alt_text":"medical alert","src":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/08\/medical_alert.png?fit=725%2C250&ssl=1&resize=350%2C200","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/08\/medical_alert.png?fit=725%2C250&ssl=1&resize=350%2C200 1x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/08\/medical_alert.png?fit=725%2C250&ssl=1&resize=525%2C300 1.5x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/08\/medical_alert.png?fit=725%2C250&ssl=1&resize=700%2C400 2x"},"classes":[]},{"id":767,"url":"https:\/\/www.groupactionlawyers.co.uk\/blog\/accu-chek-insight-insulin-pumps-battery-life-issues","url_meta":{"origin":252,"position":2},"title":"Issues with battery life of the Accu-Chek Insight insulin pumps","author":"Admin","date":"26th June 2017","format":false,"excerpt":"All Accu-Chek Insight insulin pumps have received new instructions for better device management due to previous complaints about the battery lifetime and the device having unexpected shutdowns. The first warning for the medical device was issued on the 4th August 2015 where Roche Diabetes Care, the medical manufacturers of the\u2026","rel":"","context":"In &quot;Medical&quot;","block_context":{"text":"Medical","link":"https:\/\/www.groupactionlawyers.co.uk\/blog\/category\/medical"},"img":{"alt_text":"medical alert","src":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/08\/medical_alert.png?fit=725%2C250&ssl=1&resize=350%2C200","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/08\/medical_alert.png?fit=725%2C250&ssl=1&resize=350%2C200 1x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/08\/medical_alert.png?fit=725%2C250&ssl=1&resize=525%2C300 1.5x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/08\/medical_alert.png?fit=725%2C250&ssl=1&resize=700%2C400 2x"},"classes":[]},{"id":910,"url":"https:\/\/www.groupactionlawyers.co.uk\/blog\/medtronic-under-greater-scrutiny-more-problem-products","url_meta":{"origin":252,"position":3},"title":"Medtronic under greater scrutiny as more of its products run into problems","author":"Admin","date":"30th August 2017","format":false,"excerpt":"Medical device maker Medtronic have been making the headlines for all the wrong reasons lately. Priding itself as the \"global leader in medical technology, services, and solutions\", Medtronic have been at the centre of a fair few recalls for defects and risks that have arisen from the use of their\u2026","rel":"","context":"In &quot;Latest&quot;","block_context":{"text":"Latest","link":"https:\/\/www.groupactionlawyers.co.uk\/blog\/category\/latest"},"img":{"alt_text":"alert","src":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/12\/healthcare-apps.png?fit=725%2C250&ssl=1&resize=350%2C200","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/12\/healthcare-apps.png?fit=725%2C250&ssl=1&resize=350%2C200 1x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/12\/healthcare-apps.png?fit=725%2C250&ssl=1&resize=525%2C300 1.5x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/12\/healthcare-apps.png?fit=725%2C250&ssl=1&resize=700%2C400 2x"},"classes":[]},{"id":1072,"url":"https:\/\/www.groupactionlawyers.co.uk\/blog\/medical-device-alert-datascope-corp-intra-aortic-balloon-pumps","url_meta":{"origin":252,"position":4},"title":"Medical device alert for Datascope Corp intra-aortic balloon pumps","author":"Admin","date":"8th November 2017","format":false,"excerpt":"The Medicines and Healthcare products Regulatory Agency (MHRA) has issued a medical device alert for intra-aortic balloon pumps manufactured by Datascope Corp. Models CS100, CS100i and CS300 are reportedly at risk of \"haemodynamic instability to patients with critical care conditions due to a delay in, or sudden interruption of, therapy.\"\u2026","rel":"","context":"In &quot;Medical&quot;","block_context":{"text":"Medical","link":"https:\/\/www.groupactionlawyers.co.uk\/blog\/category\/medical"},"img":{"alt_text":"alert","src":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/12\/healthcare-apps.png?fit=725%2C250&ssl=1&resize=350%2C200","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/12\/healthcare-apps.png?fit=725%2C250&ssl=1&resize=350%2C200 1x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/12\/healthcare-apps.png?fit=725%2C250&ssl=1&resize=525%2C300 1.5x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/12\/healthcare-apps.png?fit=725%2C250&ssl=1&resize=700%2C400 2x"},"classes":[]},{"id":645,"url":"https:\/\/www.groupactionlawyers.co.uk\/blog\/medical-device-lithium-ion-batteries-can-smoke-spark-dropped","url_meta":{"origin":252,"position":5},"title":"Lithium-ion batteries in a medical device can cause smoke and sparks if dropped","author":"Admin","date":"8th May 2017","format":false,"excerpt":"Damaged lithium-ion batteries in a medical device have been a cause for concern for the Medicines and Healthcare products Regulatory Agency (MHRA). The CARDIOSAVE hybrid intra-aortic balloon pump (IABP) and CARDIOSAVE rescue IABP have been reported to have damaged lithium-ion batteries that may give off smoke, a bad smell, or\u2026","rel":"","context":"In &quot;Medical&quot;","block_context":{"text":"Medical","link":"https:\/\/www.groupactionlawyers.co.uk\/blog\/category\/medical"},"img":{"alt_text":"alert","src":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/12\/healthcare-apps.png?fit=725%2C250&ssl=1&resize=350%2C200","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/12\/healthcare-apps.png?fit=725%2C250&ssl=1&resize=350%2C200 1x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/12\/healthcare-apps.png?fit=725%2C250&ssl=1&resize=525%2C300 1.5x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/12\/healthcare-apps.png?fit=725%2C250&ssl=1&resize=700%2C400 2x"},"classes":[]}],"jetpack_sharing_enabled":true,"_links":{"self":[{"href":"https:\/\/www.groupactionlawyers.co.uk\/blog\/wp-json\/wp\/v2\/posts\/252","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.groupactionlawyers.co.uk\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.groupactionlawyers.co.uk\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.groupactionlawyers.co.uk\/blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.groupactionlawyers.co.uk\/blog\/wp-json\/wp\/v2\/comments?post=252"}],"version-history":[{"count":4,"href":"https:\/\/www.groupactionlawyers.co.uk\/blog\/wp-json\/wp\/v2\/posts\/252\/revisions"}],"predecessor-version":[{"id":354,"href":"https:\/\/www.groupactionlawyers.co.uk\/blog\/wp-json\/wp\/v2\/posts\/252\/revisions\/354"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.groupactionlawyers.co.uk\/blog\/wp-json\/wp\/v2\/media\/255"}],"wp:attachment":[{"href":"https:\/\/www.groupactionlawyers.co.uk\/blog\/wp-json\/wp\/v2\/media?parent=252"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.groupactionlawyers.co.uk\/blog\/wp-json\/wp\/v2\/categories?post=252"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.groupactionlawyers.co.uk\/blog\/wp-json\/wp\/v2\/tags?post=252"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}