According to the Pennsylvania Record, a woman has filed a lawsuit against Bayer after she said she became pregnant while using a Mirena intrauterine device (IUD) because the product moved from its original spot in her body.
The news source reported that the woman, Rebecca Syx, filed the lawsuit in the U.S. District Court in Philadelphia on February 10 accusing the pharmaceutical company of negligence, defective manufacturing, defective design, strict liability, and other violations.
Syx, 33, reportedly had her doctor insert the device into her during an office visit in 2011. When she went in for a follow up appointment, the doctor confirmed that the device was still in the proper location; however, a month later the doctor discovered that Syx was pregnant.
A few days later, Syx underwent an ultrasound, which failed to locate the device. Another ultrasound subsequently reveled that the device moved to her vescio-uterine wall just posterior to the bladder and anterior to the uterus.
Syx gave birth to her child via caesarian section in early 2013, at which time the device was removed surgically from her body.
More than 2 million women in the U.S. have been implanted with Mirena IUDs, which have been linked to dislocation. Since 2008, nearly 4,800 women nationwide have reported that the device has become dislocated in them or embedded in their uteruses. The devices migrating and embedding have caused a variety of injuries, from perforations to unplanned pregnancies.
Has the Mirena IUD Device Injured You?
If you have been injured because of a Mirena IUD, we can help you. Contact our attorneys who are experienced in multidistrict litigation and defective medical devices. Call toll-free (888)841-9623 today.
Zoll, Kranz & Borgess, LLC – Mirena IUD attorneys
Michelle is a founding partner of Zoll & Kranz, located in Toledo, Ohio. Michelle has been a plaintiff’s lawyer for the entirety of her practice – over 32 years. She devotes the majority of her time to complex consolidated litigation and class action including advocating for people injured by medical devices, prescription medications, or corporate negligence.
This article has been written and reviewed for legal accuracy and clarity by the team of writers and attorneys at Zoll & Kranz, LLC and is as accurate as possible. This content should not be taken as legal advice from an attorney. If you would like to learn more about our owner and experienced Ohio injury lawyer, Michelle L. Kranz, you can do so here.
Zoll & Kranz, LLC does everything possible to make sure the information in this article is up to date and accurate. If you need specific legal advice about your case, contact us. This article should not be taken as advice from an attorney.
A serious injury can have life-altering results.
Don’t settle for less than you deserve, speak with an award-winning personal injury lawyer today.
FDA Warns Pfizer’s Drug Tygacil Raises Risk of Death
FDA Announces da Vinci Surgical System Robot Recall
FDA Issues Warning Over Phillips Heart Defibrillators
FDA Issues Warning About Medtronic Guidewire Recall
Unsterile Medical Device Recall: Zoll & Kranz, LLC is investigating the Seprafilm Class II Recall
For over 37 years, Zoll & Kranz has been fighting for clients who have been the victims of the wrongful death of a loved one.
Do you believe you’re entitled to compensation?
Use our Instant Case Evaluator to find out in as little as 60 seconds!
A serious injury can have life-altering results.
Don’t settle for less than you deserve, speak with an award-winning personal injury lawyer today.