For countless women across the country, defective transvaginal mesh implants have been linked to serious complications, including erosion, exposure, or extrusion of the mesh, recurrent pelvic organ prolapse (POP), recurrent stress urinary incontinence (SUI), pain, infection, bleeding, vaginal scarring, and painful sexual intercourse.
After suffering because of a transvaginal mesh implant, many women have filed injury lawsuits, a number of which have been successful. Several manufacturers, including Endo International Plc, have agreed to settlements, while some, including C.R. Bard, Boston Scientific and Cook Medical Systems, are fighting the cases in court.
The Charleston Daily Mail recently reported on one such case: Jo Huskey and her husband, Allen Huskey, filed a case in federal court against Ethicon Inc. and Johnson & Johnson. According to the suit, Mrs. Huskey had an implant placed in her in Illinois and she now suffers from SUI (stress urinary incontinence ), along with other health problems. She is seeking damages for negligence, manufacturing defects, negligent misrepresentation, and other claims.
Huskey’s case is the second to go to trial against Ethicon. U.S. District Judge Joseph Goodwin is overseeing thousands of other similar cases, which have been transferred to his West Virginia court.
Right now, transvaginal mesh manufacturers are being forced to conduct safety studies by the U.S. Food and Drug Administration (FDA) due to the high number of adverse events associated with the devices.
If you have suffered an injury because of a transvaginal mesh device, you should speak to our attorneys immediately, as there have been deadlines associated with suits and settlements.
Zoll & Kranz, LLC – Defective Medical Drug and Device Lawyers
ZK’s ‘Did You Know’? Stress urinary incontinence can cause someone to leak urine during physical activities, even while just coughing or sneezing.
Source: http://www.charlestondailymail.com/article/20140826/DM02/140829504
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.