UPDATE: 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.
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