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Arlington Heights defective medical device attorneyUPDATE: The recall discussed below, which took place in 2014, was for two lots of ParaGard devices that were not known to be fully sterile. The ParaGard IUD has never been subject to a full recall. However, in the years since this recall, many patients have reported issues with the devices, and multiple lawsuits are currently pending against the manufacturer.

The primary issue that has been reported with the ParaGard IUD is the possibility that it will break, usually when being removed from a patient's uterus. This can leave fragments of the device inside a person's body, and these fragments may need to be surgically removed to prevent further damage to the uterus or other organs. Since 2013, there have been more than 3,000 reports of device breakage made to the Food and Drug Administration (FDA). Nearly 2,000 of these events were considered serious, and 102 people have been hospitalized or faced life-threatening complications. It is likely that the issue is much more widespread, since there are many more people who have not reported incidents to the government or who are unaware of the risks they may face.

While the FDA has not indicated that it will be conducting investigations into the safety of ParaGard IUDs, some online communities are working together to help people share their experiences and raise awareness of the risks people face. In addition, at least 55 lawsuits have been filed in 20 different states by women who have suffered injuries because of the breakage of these devices. If you have experienced any injuries or health issues related to ParaGard IUDs or other birth control devices, Newland & Newland, LLP can advise you of your legal options and help you take action to recover financial compensation. Contact our Schaumburg personal injury lawyers today at 847-797-8000 to arrange a free consultation.


According to Fox News, more than 3,600 women have joined together to file an unsafe medical drug lawsuit against drug manufacturer Merck. According to the lawsuit, more than 100 women have died as a result of using the company's contraceptive, NuvaRing.

Lawyers associated with the suit argue that the contraceptive ring caused blood clots that resulted in death. They also state that Merck failed to include the risk of clots on the medication label and did not inform doctors that NuvaRing carries a clotting risk that is up to five times greater than traditional birth control pills.

NuvaRing uses a different type of progestin than what is contained in other birth control medications. Desogestrel and its related compounds carry fewer side effects (such as acne) than birth control pills but carry a higher risk of blood clots. According to research in the British Medical Journal, vaginal rings also carry a 90 percent greater risk of venous thromboembolism (a blood clot that blocks a vein).


The NuvaRing, a contraceptive device originally marketed as a safe alternative to traditional birth control pills has not been officially recalled, despite rumors that it has been. According to PR Newswire, at the beginning of this year the trial date for 1,000 lawsuits involving the device was extended, “feeding rumors that the vaginal ring contraceptive's manufacturer, Merck, may be ready to enter settlements negotiations,” reports PR Newswire. Approximately 1.5 million women worldwide use the device despite increased risk.

The increased risks of NuvaRing include increased chance of blood clots, pulmonary embolism, and strokes. According to the Huffington Post, the FDA, after clinical trials in which “a healthy woman in her 20s had developed a blood clot—a surprising occurrence that an investigator determined was probably related to the birth control device,” said that the manufacturer needed to include warnings with the NuvaRing packaging. Manufacturer Organon, “adamantly opposed such a statement,” according to the Huffington Post.

Organon, the Huffington Post reports, was planning to market NuvaRing as a safe alternative to birth control pills, with fewer side effects. “An elevated VTE [venous thromboembolism] warning label would have been a huge blow,” according to the Huffington Post. “Such a warning might have discouraged women from using NuvaRing and made doctors less inclined to prescribe it—significantly cutting into the potential return on investment,” the Huffington Post reports.


NuvaRing Trial Date Postponed

Posted on February 08, 2013 in Birth Control

Yahoo! Finance is reporting that the scheduled May 2013 trial date in the multidistrict NuvaRing litigation, which is currently pending before the U.S. District Court, Eastern District of Missouri, has been postponed. This latest continuance of the trial proceedings has resulted in rumors that Merck, the manufacturer of the vaginal ring contraceptive, is preparing to enter into settlement negotiations. Not only does this development raise the potential for much-needed financial relief for women injured by using NuvaRing, but it also leaves open the possibility that even more lawsuits will be added to the more than 1,000 NuvaRing lawsuits that already are pending.

NuvaRing was the first vaginal hormonal contraceptive device approved by the U.S. Food & Drug Administration (FDA) in 2001. The ring works by releasing a low dose of synthetic progestin and estrogen over a period of three weeks. Starting in May, 2007, consumers began to file complaints in jurisdictions nationwide claiming dangerous side effects from using the medical device. Studies in 2009 and 2011 reveal that using NuvaRing considerably increases the risk of serious blood clots, including a 56% increased risk of deep vein thrombosis and pulmonary embolism over those women who use regular birth control pills. To date, the FDA has received almost 5,000 adverse event reports from users of NuvaRing. Nonetheless, NuvaRing has not been recalled from U.S. markets, and 1.5 million women worldwide continue to use NuvaRing.

If you or a loved one has suffered injuries or dangerous side effects from using NuvaRing, there still may be time to file a claim in the pending litigation. You may be entitled to damages for the injuries that you have sustained that are attributable to NuvaRing. For more information about the NuvaRing litigation and other defective medical devices, contact your Illinois defective medical device attorney today.

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