{"id":8505,"date":"2013-03-04T22:41:00","date_gmt":"2013-03-04T22:41:00","guid":{"rendered":"https:\/\/taylormartino.com\/?p=8505"},"modified":"2022-09-13T19:33:55","modified_gmt":"2022-09-13T19:33:55","slug":"granuflo-and-naturalyte-recalled-by-the-fda","status":"publish","type":"post","link":"https:\/\/taylormartino.com\/granuflo-and-naturalyte-recalled-by-the-fda\/","title":{"rendered":"GranuFlo and Naturalyte Recalled by the FDA"},"content":{"rendered":"\r\n<ul class=\"wp-block-gallery columns-1 is-cropped wp-block-gallery-1 is-layout-flex wp-block-gallery-is-layout-flex\">\r\n<li class=\"blocks-gallery-item\">\r\n<figure id=\"attachment_8508\" aria-describedby=\"caption-attachment-8508\" style=\"width: 800px\" class=\"wp-caption alignnone\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-8508 \" src=\"https:\/\/taylormartino.com\/wp-content\/uploads\/2013\/03\/GranuFlo-and-Naturalyte-Recalled-by-the-FDA-300x200.jpg\" alt=\"GranuFlo and Naturalyte Recalled by the FDA\" width=\"800\" height=\"533\" data-id=\"7189\" data-link=\"https:\/\/taylormartino.com\/?attachment_id=7189\" srcset=\"https:\/\/taylormartino.com\/wp-content\/uploads\/2013\/03\/GranuFlo-and-Naturalyte-Recalled-by-the-FDA-300x200.jpg 300w, https:\/\/taylormartino.com\/wp-content\/uploads\/2013\/03\/GranuFlo-and-Naturalyte-Recalled-by-the-FDA-768x512.jpg 768w, https:\/\/taylormartino.com\/wp-content\/uploads\/2013\/03\/GranuFlo-and-Naturalyte-Recalled-by-the-FDA.jpg 1000w\" sizes=\"(max-width: 800px) 100vw, 800px\" \/><figcaption id=\"caption-attachment-8508\" class=\"wp-caption-text\">GranuFlo and Naturalyte Recalled by the FDA<\/figcaption><\/figure>\r\n<\/li>\r\n<\/ul>\r\n\r\n\r\n\r\n<span class=\"gdlr-core-space-shortcode\" style=\"margin-top: 30px ;\"  ><\/span>\r\n<p>On March 29<sup>th<\/sup>, 2012, the U.S. Food and Drug Administration (FDA) issued a <strong>Class I recall<\/strong> on the drug GranuFlo Dry Acid Concentrate and Naturalyte Liquid Acid Concentrate. (Class I recalls are the most serious type of recall and involve situations in which there is a reasonable probability that use of these products will cause serious adverse health consequences or death.) GranuFlo and Naturalyte are alkaline substances administered to dialysis patients to neutralize the acid that builds up in the blood. The products are administered in conjunction with bicarbonate, and contain acetate, an ingredient that the body converts to bicarbonate. However, GranuFlo and Naturalyte contain far more acetate than rival products and thus result in more bicarbonate in the body. Research shows that high bicarbonate levels can cause a variety of health problems including:<\/p>\r\n<ul>\r\n<li>Cardiopulmonary arrest<\/li>\r\n<li>Heart problems<\/li>\r\n<li>Metabolic alkalosis<\/li>\r\n<li>Low blood pressure<\/li>\r\n<li>Sudden MI or heart attack<\/li>\r\n<li>Stroke, and<\/li>\r\n<li>Death<\/li>\r\n<\/ul>\r\n<p>An internal memo from Fresenius Medical Care, the manufacturer of Granuflo and Naturalyte, warned that failure to account for an excess of bicarbonate resulting from an ingredient contained in their product, GranuFlo, was associated with \u201c\u20266 to 8 greater risk of cardiopulmonary arrest and sudden cardiac death in the dialysis facility.\u201d \u00a0The memo also stated that 941 patients suffered cardiac arrest inside the Fresenius Clinics in 2010.<\/p>\r\n<p>If you or any family members have received GranuFlo Dry Acid Concentrate and Naturlyte Liquid Acid Concentrate please give us a call at 1-800-256-7728 for a free consultation and evaluation.<\/p>\r\n<p>Recall Notice<\/p>\r\n\r\n\r\n\r\n<span class=\"gdlr-core-space-shortcode\" style=\"margin-top: 40px ;\"  ><\/span>\r\n\r\n\r\n\r\n<figure class=\"wp-block-embed-youtube aligncenter wp-block-embed is-type-video is-provider-youtube wp-embed-aspect-16-9 wp-has-aspect-ratio\">\r\n<div class=\"wp-block-embed__wrapper\"><div class=\"yrc-shell-cover yrc-single\" data-yrc-uid=\"67436c13bf903\" data-yrc-channel=\"{&quot;meta&quot;:{&quot;user&quot;:&quot;Taylor Martino Rowan Personal Injury 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class=\"gdlr-core-space-shortcode\" style=\"margin-top: 40px ;\"  ><\/span>\r\n","protected":false},"excerpt":{"rendered":"<p>On March 29th, 2012, the U.S. Food and Drug Administration (FDA) issued a Class I recall on the drug GranuFlo Dry Acid Concentrate and Naturalyte Liquid Acid Concentrate. (Class I recalls are the most serious type of recall and involve situations in which there is a reasonable probability that use of these products will cause [&hellip;]<\/p>\n","protected":false},"author":3,"featured_media":8508,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[95],"tags":[99,10,13,16],"class_list":["post-8505","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-news","tag-dangerous-product","tag-general-practice","tag-law","tag-personal-injury"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v23.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>GranuFlo and Naturalyte Recalled by the FDA<\/title>\n<meta name=\"description\" content=\"The FDA issued a Class I recall on the drug GranuFlo Dry Acid Concentrate and Naturalyte Liquid Acid Concentrate given to dialysis patients.\" \/>\n<meta name=\"robots\" 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