{"id":5946,"date":"2012-12-04T16:54:40","date_gmt":"2012-12-04T21:54:40","guid":{"rendered":"http:\/\/localhost:10028\/practiceareas\/new-york-zimmer-biomet-bone-growth-spinal-fusion-stimulator-lawyers\/"},"modified":"2022-06-21T16:54:56","modified_gmt":"2022-06-21T20:54:56","slug":"new-york-zimmer-biomet-kemik-buyumesi-spinal-fuzyon-stimulatoru-avukatlar","status":"publish","type":"practiceareas","link":"https:\/\/napolilaw.lemonadestand.org\/tr\/uygulama-alanlari-2\/new-york-zimmer-biomet-kemik-buyumesi-spinal-fuzyon-stimulatoru-avukatlar\/","title":{"rendered":"Zimmer Biomet Kemik B\u00fcy\u00fcmesi ve Spinal F\u00fczyon Stim\u00fclat\u00f6r\u00fc"},"content":{"rendered":"

Kas\u0131m 2018'de G\u0131da ve \u0130la\u00e7 \u0130daresi, daha \u00f6nceki bir Zimmer Biomet Kemik B\u00fcy\u00fcmesi ve Spinal F\u00fczyon Stim\u00fclat\u00f6r\u00fc geri \u00e7a\u011fr\u0131s\u0131n\u0131 S\u0131n\u0131f I Geri \u00c7a\u011f\u0131rmaya y\u00fckseltti. FDA bu eylemi yaln\u0131zca "ihlal edici bir \u00fcr\u00fcn\u00fcn kullan\u0131m\u0131n\u0131n veya bu \u00fcr\u00fcne maruz kalman\u0131n makul bir olas\u0131l\u0131kla ciddi olumsuz sa\u011fl\u0131k sonu\u00e7lar\u0131 veya \u00f6l\u00fcm<\/a>.\u201d Issues with the Bone Growth\/Spinal Fusion Stimulator mainly include a lack of validation which can cause serious, and possibly fatal, bacterial infections.<\/p>\n

This latest recall is just the latest in a strong of difficulties for Zimmer Biomet and the entire medical device industry. In 2017, a study linked cheap foreign components in hip implants with beyin yaralanmalar\u0131<\/a>. As a result of these supply chain problems and other challenges, Zimmer Biomet\u2019s CEO resigned.<\/p>\n

FDA officials knew about the Bone Growth\/Spinal Fusion Stimulator\u2019s issues for almost a year before they issued a recall. When government bureaucrats refuse to protect consumers, the assertive attorneys at Napoli Hukuku<\/a> bo\u015flukta dur. Kollar\u0131m\u0131z\u0131 s\u0131vay\u0131p, tazminat talebinizi destekleyen kan\u0131tlar\u0131 topluyoruz. Ard\u0131ndan, mahkemede zorlay\u0131c\u0131 bir dava sunuyoruz. Uzmanl\u0131\u011f\u0131m\u0131z nedeniyle, kusurlu t\u0131bbi cihaz davalar\u0131m\u0131z\u0131n \u00e7o\u011fu mahkeme d\u0131\u015f\u0131nda \u00e7\u00f6z\u00fcl\u00fcr. B\u00fcy\u00fck t\u0131bbi cihaz \u015firketleri hukuk ekibimizden korkuyor ve biz de bu ger\u00e7e\u011fi kendi avantaj\u0131n\u0131za kullan\u0131yoruz.<\/p>\n

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Zimmer biomet Kemik B\u00fcy\u00fcmesi\/Spinal F\u00fczyon Stim\u00fclat\u00f6r\u00fc nedir?<\/h2>\n

This device uses small electrical impulses to stimulate bone growth. Doctors typically use the Bone Growth\/Spinal Fusion Stimulator to facilitate faster recovery from spinal fusion surgery or a serious broken bone. This gadget may have some off-label uses as well, most notably in certain kinds of dental procedures.<\/p>\n

In 2017, the FDA began receiving complaints from patients who had this device implanted and experienced severe bacterial infections. But rather than take action, the FDA did nothing. Instead, it allowed Zimmer\/Biomet to issue a voluntary recall in February 2018.<\/p>\n

Two months later, FDA officials re-inspected the company\u2019s Bone Growth\/Spinal Fusion Stimulator production facility, and they were aghast at what they found. The company had apparently done little or nothing to correct the flaws in the manufacturing process. Zimmer Biomet officials said the problems were a \u201cmisunderstanding\u201d and promised further corrective action. Rather unsurprisingly, that action did not materialize.<\/p>\n

Nevertheless, the FDA waited another six months to issue a recall. That notice was backdated to Bone Growth\/Spinal Fusion Stimulator which hit the market beginning in 2015. So, anyone who received a Zimmer Biomet Bone Growth\/Spinal Fusion Stimulator between 2015 and 2018 is at risk for serious injury.<\/p>\n

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Yayg\u0131n T\u0131bbi Bakteriyel Enfeksiyonlar<\/h2>\n

There is little anyone can do about sporadic, one-off bacterial infections. Understandably, manufacturers may not be liable for damages in these situations. But a chronic lack of oversight is a different matter. If the device is defective, people get hurt, and the company does nothing, liability may attach as outlined below.<\/p>\n

The bacterial infections which result from a lack of control can cause serious and fatal conditions. The most common types of device-related infections are:<\/p>\n