![]() ![]() You will continue to receive generic ads. ![]() Our ad network partner uses cookies and Web beacons to collect non-personally identifiable information about your activities on this and other Web sites to provide you targeted advertising based upon your interests. Please note this does not opt you out of being served advertising. We partner with a third party ad network to either display advertising on our Web site or to manage our advertising on other sites. You should contact our firm or other lawyers to verify any information. Our website has always been intended to be informational in nature and not to provide legal advice. The Firm is in the process of amending much of the content on the website to conform to these new laws. Several other legal rights were amended or removed as well. The Florida legislature passed a series of new laws in March 2023 that, for example, reduced the statute of limitations (the time in which you have to file a lawsuit) for negligence cases from (4) years to (2) years. If you have questions and would like to speak with an attorney, please call 80 or contact us online to schedule a free initial consultation. Our firm has decades of experience successfully pursuing claims against Johnson & Johnson and other companies for serious and fatal injuries resulting from defective medical devices. Schedule a Free Initial Consultation at Searcy Denney Unfortunately, issues with defective medical devices are common, and individuals and families are often forced to take legal action in order to hold manufacturers such as Ethicon and Johnson & Johnson accountable. If you or a loved one has been or may have been harmed, by a defective Proximate® reloadable surgical stapler, we would encourage you to speak with a lawyer about your legal rights. What Should You Do if You or a Loved One was Harmed by a Defective Surgical Stapler? In the letter, the FDA states that it received more than 41,000 reports related to surgical staplers between Januand March 31, 2018, including reports of more than 9,000 serious injuries and 366 deaths. Shortly before Ethicon issued the recall, the FDA sent a letter to health care providers warning of an increase in the number of adverse events associated with surgical staplers in general. Life-long nutritional and digestive issues.The need for additional closures (anastomoses).The need for additional imaging studies.The FDA states that potential risks to patients who underwent gastrointestinal surgeries performed with Ethicon’s Proximate® reloadable staplers include: ![]() Failure to cut the washer suggests complete 360-degree staple line failure.” The FDA’s recall notice from May 2019 states that Ethicon has confirmed “serious injuries to two patients,” and also notes that the recall was triggered by the investigation of multiple complaints and returned products. due to insufficient firing, which can compromise staple line integrity. In describing the reason for the recall, the FDA writes that Ethicon has confirmed, “uncut washers in the stapler and malformed staples occur. Proximate® Reloadable Surgical Staplers Recalled Due to a Critical Flaw Ethicon distributed the staplers to health care providers between Maand March 8, 2019. Just over a month later, more than 92,000 Proximate® reloadable surgical staplers had been recalled. ![]() Food and Drug Administration has classified the recall as a Class I recall, which means that, “there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.”Īccording to the FDA, Ethicon recalled the devices, also known as endo-surgery endoscopic curved intraluminal staplers and endo-surgery endoscopic curved intraluminal staplers, on April 11, 2019. In 2019, Johnson & Johnson subsidiary Ethicon issued a recall for its Proximate® reloadable surgical staplers due to a flaw with the device that may have resulted in staple lines being compromised during gastrointestinal surgeries. ![]()
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