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Author Archives: Jane Akre

How to Look Up Your Pelvic Mesh Case

By Mesh Medical Device Newsdesk |

                  Mesh Medical Device News Desk, January 2, 2017 ~ Many of you already know how to look up your pelvic mesh case filed in federal court. Here is a step-by-step way to find it through a Google Search. This applies only to the cases consolidated [continue reading…]

2016 – The Mesh Year in Review

By Mesh Medical Device Newsdesk |

Mesh Medical Device News Desk, December 29, 2016 ~ It may not seem like much has happened in the world of polypropylene mesh implants this year, but a review of 2016 tells otherwise. There have been changes and shifts in litigation and research, albeit moving much too slowly for the 100,000 or so mesh-injured patients [continue reading…]

Wishing You All the Best This Holiday and for the New Year!

By Mesh Medical Device Newsdesk |

Mesh News Desk, December 23, 2016~   I wanted to take this opportunity to thank all of you who visit Mesh Medical Device News Desk and find it a valuable community. It’s my honor to provide you with news and information and to speak with many readers during the year.  Thank you for sharing [continue reading…]

Is Your Lawyer Helping To Resolve Your Pelvic Mesh Lawsuit?

By Mesh Medical Device Newsdesk |

Mesh Medical Device News Desk, December 21, 2016~ Is your law firm responsive to your questions pertaining to your pelvic mesh lawsuit?  Do they return your calls?  Have you received your settlement?   Recently “Suzy” called your editor with a concern ( she does not want her real name used because she is represented [continue reading…]

Mullins Pelvic Mesh Trial Set for March

By Mesh Medical Device Newsdesk |

Mesh Medical Device News Desk, December 20, 2016 ~ After much delay, the Mullins case, a defective pelvic mesh trial of 31 women, is scheduled for March of next year.   Mullins has been set many times before, but it appears that Judge Joseph Goodwin has finally set March 6, 2017 as the first [continue reading…]

What is Multidistrict Litigation?

By Mesh Medical Device Newsdesk |

Mesh Medical Device News Desk, December 16, 2016 ~ MDL, Multidistrict Litigation.  Readers of Mesh Medical Device News Desk have been hearing about the court where most of the transvaginal mesh cases are consolidated. But what is the MDL and how did it get started? In early January 2012, the number of transvaginal pelvic mesh [continue reading…]

Ten Deaths Associated With J&J Physiomesh Hernia Mesh

By Mesh Medical Device Newsdesk |

Mesh Medical Device News Desk, December 15, 2016 ~ At least 10 deaths and seven injuries, associated with PHYSIOMESH™ (JNJ) hernia mesh, have been reported to the U.S. Food and Drug Administration (FDA). Device Events worked with Mesh News Desk in preparation of this story. Civil lawsuits that become mass torts involving many plaintiffs, [continue reading…]

Study Confirms The More Transvaginal Pelvic Mesh The More Mess

By Mesh Medical Device Newsdesk |

Mesh Medical Device News Desk, December 12, 2016 ~ A study published in JAMA Surgery confirms the  common adage among the mesh aware community, the more transvaginal  pelvic mesh present in a body, the more likely there will be complications. The question posed by the study is – What is the association between the [continue reading…]

Linda Gross $11.1 Mill Jury Verdict Survives Final J&J Challenge

By Mesh Medical Device Newsdesk |

Mesh Medical Device News Desk, December 6, 2016 ~ J&J appeal to the New Jersey Supreme Court has been rejected for consideration. It was the last appeal for Johnson & Johnson.  It was February 2013 when South Dakota nurse, Linda Gross was awarded $11.1 by an Atlantic City New Jersey jury after a seven-week [continue reading…]

FDA Pelvic Mesh Data – Are Thousands of Deaths Not Being Reported?

By Mesh Medical Device Newsdesk |

Mesh Medical Device News Desk, December 5, 2016 ~ A former FDA IT project manager left the agency to focus on patient safety and the numbers needed for true patient advocacy. Imagine 5.6 million pieces of data collected by the U.S. Food and Drug Administration (FDA) concerning adverse events, the FDA term for complications. [continue reading…]

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