BioSpace Collaborative

Academic/Biomedical Research
News & Jobs
Biotechnology and Pharmaceutical Channel Medical Device and Diagnostics Channel Clinical Research Channel BioSpace Collaborative    Job Seekers:  Register | Login          Employers:  Register | Login  

NEWSLETTERS
Free Newsletters
Archive
My Subscriptions

NEWS
News by Subject
News by Disease
News by Date
PLoS
Search News
Post Your News
JoVE

CAREER NETWORK
Job Seeker Login
Most Recent Jobs
Search Jobs
Post Resume
Career Fairs
Career Resources
For Employers

HOTBEDS
Regional News
US & Canada
  Biotech Bay
  Biotech Beach
  Genetown
  Pharm Country
  BioCapital
  BioMidwest
  Bio NC
  BioForest
  Southern Pharm
  BioCanada East
  C2C Services & Suppliers™
Europe
Asia

DIVERSITY

PROFILES
Company Profiles

INTELLIGENCE
Research Store

INDUSTRY EVENTS
Research Events
Post an Event
RESOURCES
Real Estate
Business Opportunities

 News | News By Subject | News by Disease News By Date | Search News
Get Our Industry eNewsletter FREE email:    
   

N.J. Woman Sues Johnson & Johnson (JNJ)'s Ethicon, Inc. (JNJ) Unit Over Vaginal Mesh Injuries, Says The Lanier Law Firm


6/13/2012 10:08:50 AM

ATLANTIC CITY, N.J., June 12, 2012 /PRNewswire/ -- A woman who suffered significant injuries after being implanted with a defective vaginal mesh patch has filed a lawsuit against New Brunswick, N.J.-based healthcare giant Johnson & Johnson (NYSE:JNJ) and a company subsidiary.

Attorneys from The Lanier Law Firm filed the complaint on June 11, 2012, for New Jersey resident Elizabeth Matthews against Johnson & Johnson and company subsidiary Ethicon Inc. of Somerville, N.J., in the Superior Court of New Jersey in Atlantic City. The case is Matthews v. Ethicon Inc., et al., No. ATL-L-4054-12.

Ms. Matthews was implanted with Ethicon's Gynecare Prolift and TVT Secur products during a surgical procedure performed in November 2007. After receiving the implants, she suffered various internal injuries and assorted health problems that persist to this day.

Earlier this month, Johnson & Johnson announced a request filed with the U.S. Food and Drug Administration (FDA) to stop selling the Gynecare Prolift, Prolift+ M, TVT Secur and Prosima surgical mesh products. In March, the FDA announced that Johnson & Johnson sold the Gynecare Prolift product for three years without proper regulatory approval. The FDA earlier ordered Johnson & Johnson and several other vaginal mesh implant manufacturers to study organ damage and other health problems associated with the products.

The Lanier Law Firm represents numerous victims of defective vaginal mesh implants in the mass tort litigation pending in New Jersey and the multidistrict litigation pending in the U.S. District Court for the Southern District of West Virginia. The firm currently is investigating potential legal claims involving similar products manufactured by Bard Medical, American Medical Systems and Boston Scientific.

Led by noted trial lawyer Mark Lanier, The Lanier Law Firm is widely recognized as one of the nation's top plaintiffs' law firms, including experience in cases involving dangerous pharmaceutical drugs, defective medical products and toxic exposure.

With offices in Houston, Los Angeles, New York, and Palo Alto, The Lanier Law Firm is committed to addressing client concerns with effective and innovative solutions in courtrooms across the country. The firm is composed of outstanding trial attorneys with decades of experience handling cases involving pharmaceutical liability, asbestos exposure, intellectual property, business litigation, product liability, maritime law, bad faith insurance claims, and sports and entertainment law. Visit http://www.lanierlawfirm.com.

For more information on the vaginal mesh lawsuit against Johnson & Johnson, please contact J.D. Cargill at 713-659-5200.

SOURCE The Lanier Law Firm


Read at BioSpace.com


   

ADD TO DEL.ICIO.US    ADD TO DIGG    ADD TO FURL    ADD TO STUMBLEUPON    ADD TO TECHNORATI FAVORITES
 

//-->