YOU MAY BE ENTITLED TO COMPENSATION AND DAMAGES FOR YOUR INJURIES – WE ARE AVAILABLE TO ASSIST YOU IN YOUR RECOVERY
Lawsuits Are Being Filed Against Bayer, the Makers of Essure Implants, Claiming Serious Complications
According to class action lawsuits filed nationwide, Essure has caused women painful menstrual periods, perforated fallopian tubes, and migration of the device to other nearby organs
If you or a family member has or have had Essure implants and have been injured, you may be entitled to compensation.
ESSURE IMPLANT ALERT
- Our firm is vigorously pursuing this matter.
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CONTACT US NOW! Do Not Delay As The Applicable Statute Of Limitations May Result In A Complete Bar To Your Claim Regardless Of Its Merit.
About Essure Implants
Essure is a permanent contraceptive implant device. The device is a small metal polyester coil which is placed in a woman’s fallopian tubes causing complete and permanent sterilization without a surgical procedure. It works but creating inflammation in the tubes creating scar tissue which blocks the fallopian tubes passage ways. Essure was originally manufactured by Conceptus, which Bayer acquired in 2013.
The Essure implant was approved by the FDA in 2002. According to the FDA, there have been more than 4,000 events reported including severe back pain, painful and prolonged menstrual periods and pierced fallopian tubes which caused the device to be lodged in nearby organs.
Essure can cause serious complications including painful menstrual periods, vaginal bleeding, perforated fallopian tubes, device expulsion, device migration and extreme pain during intercourse. Women who have suffered adverse effects through the use of Essure have filed class action lawsuits claiming the device is defective and caused them injury. Plaintiffs also allege that Bayer took part in misleading marketing and failed to warn the public of the potential dangerous side effects of Essure. In fact, in April 2015 the FDA opened an investigation amid allegations Bayer falsified and changed the medical records during clinical trials, failed to report negative results, deceived the public and the FDA about device safety and efficiency; and used defective materials during the manufacturing process.
