If you have had a ParaGard IUD placed, or are in the process of having one, you may want to consider hiring a ParaGard IUD removal lawyer. This medical device can cause serious complications and even lawsuits, and a lawyer can help you get the compensation you need.
Partial ParaGard IUD removal
Partial ParaGard IUD removal is a simple procedure in which a small instrument is inserted into the vagina and pulled out from under the device. Although this procedure is easy, it can cause pain and bleeding afterward. Some women may also experience cramping or dizziness. If this is the case, the procedure should be performed by a doctor. After the procedure, patients can go home. In some cases, the Paragard may break during removal. Broken devices may be difficult to remove, or they may embed themselves in tissues or organs. If this happens, women may need to have their Paragard removed by surgery.
Women who have had Paragard inserted should be monitored closely to monitor for complications. If the patient experiences symptoms of recurrent endometritis, or has any other abnormalities or infections, they should immediately contact their healthcare provider. This may be the sign that the device has become infected. In these cases, antibiotics may be needed to treat the infection.
Missing two coil arms
The ParaGard IUD is a contraceptive device that is placed in a woman’s uterus. The healthcare provider inserts the device using a plastic tube and may use forceps to remove the ParaGard. As it is removed from the uterus, the arms will fold upward. The removal process is usually painless but it may cause cramping or light bleeding. If this occurs, the health care provider may prescribe a nonsteroidal anti-inflammatory drug to reduce the discomfort.
Some women may prefer to remove their IUD themselves. However, they may not be able to schedule an appointment in time. Others may want the comfort of having someone else perform the procedure. Either way, it is important to ask your health care provider to keep the IUD string long after removal.
Fortunately, removal of the Paragard IUD is a relatively straightforward and painless procedure. The procedure is performed during an office visit and does not usually require anesthesia or surgery. The procedure lasts about ten minutes and is similar to the procedure used to insert the IUD. During the removal process, the health care provider will gently pull on the IUD strings until it slides out of the uterus.
Class action lawsuits
Paragard IUD lawsuits have recently been filed in the Northern District of Georgia. These lawsuits claim that the popular IUD failed to work properly and caused a number of complications. As a result, a number of women and their families have decided to file a lawsuit against the manufacturer.
These lawsuits claim that Paragard IUDs are defective and can cause serious injuries when the coil is removed. They claim that the manufacturers of the IUD, Teva Pharmaceuticals, knew of the risks associated with their products but did not warn patients. However, the lawsuits are not class actions, since a class action would result in a single compensation that would be distributed among all plaintiffs. Instead, a multidistrict litigation process is utilized in order to determine compensation for each plaintiff.
Paragard IUD lawsuits are filed in many states. One Florida woman filed a lawsuit against Teva Pharmaceuticals after her IUD failed to work as promised. After a year of use, she was unable to conceive and suffered severe complications. She had to undergo surgery to have the device removed.
Teva Pharmaceuticals’ denial of risks
ParaGard IUD lawsuits allege that the manufacturers of the device failed to adequately warn consumers of the risks associated with the device. As a result, paragard lawsuits claim that Teva was negligent in failing to warn consumers of these risks.
Plaintiffs are currently pursuing ParaGard IUD class action litigation in federal court. The class action lawsuit has already gathered more than 1,300 plaintiffs and defendants. It has been scheduled for trial in 2024. The first bellwether trial will focus on the design flaw in the ParaGard IUD and whether or not the manufacturers knew about the flaw in the device.
Despite the fact that the device was approved by the Food and Drug Administration, Paragard has been linked to a high number of injuries. The FDA has warned that women should avoid the device and seek removal from their doctor. Further, women may be at risk for uterine rupture during the removal process.