Category Archives: Transvaginal mesh

Featured Stories

Study Linking Z-Pak to Increased Death Risk Being Reviewed by FDA

The U.S. Food & Drug Administration (FDA) is reviewing a new study that reported an increased risk of sudden, heart-related deaths among people using the antibiotic Zithromax (azithromycin), known popularly as Z-Pak. In a statement issued late yesterday, the FDA said patients being treated with Zithromax should not stop taking ...

Read More

Louisiana Whistleblower Lawsuit Revived

Louisiana Whistleblower Lawsuit Revived

A state appeals court in Louisiana has ruled that a former employee of Rapides Parish Coliseum can proceed with a whistleblower lawsuit against the Coliseum Authority.

Read More

Study Finds Metal-on-Metal Hip Implants Associated with High Incidence of Pseudotumors

Yet another study is adding to concerns about the potential dangers associated with metal-on-metal hip implants. The study, published in the Journal of Bone and Joint Surgery, found that large diameter metal-on-metal total hip replacement may be associated with a substantially higher incidence of pseudotumor formation.

Read More

FDA Advisory Panel Wrestling with Metal-on-Metal Hip Replacement Safety

An advisory panel for the U.S. Food & Drug Administration (FDA) began a highly-anticipated meeting yesterday to discuss the safety of metal-on-metal hip implants. Among other things, the panel of outside experts is being asked to make recommendations regarding the best practices for monitoring patients with metal-on-metal hip replacements. ...

Read More

First DePuy ASR Hip Implant Lawsuits Head to Trial in December, January

The first trials involving lawsuits filed against DePuy Orthopaedics by recipients of its recalled ASR Hip Implants will begin later this year, and early next year. The first is slated to start on December 3, 2012 in state court in Las Vegas, Nevada. A second DePuy ASR hip implant lawsuit ...

Read More

New York Property Owners Challenge Binghamton Fracking Ban

According to a Reuters report, the landowners believe the Binghamton, N.Y., city council and Mayor acted against proper protocol when voting to ban fracking drilling the the city. Instead, they feel the city should have consulted with the Broome County Planning Commission before approving the ban.

Read More

Medtronic Plans Layoffs, as Infuse Bone Graft Controversy Continues to Weigh on Spinal Business

Medtronic’s spinal division continues to take a huge hit thanks to the controversy surrounding its Infuse Bone Graft product. According to a report from MassDevice.com, the company’s latest earnings report stated that the division saw Infuse sales decline 26% in the first quarter of 2012, and now Medtronic is talking ...

Read More

Stryker Metal Hip Implant Component Recall Bad News for Makers of Metal-on-Metal Hip Replacement Devices

Stryker’s recent recall of two metal hip implant components, the Rejuvenate Modular and ABG II modular-neck hip stems, may have dealt a serious blow to one of the key arguments medical device manufacturers have made to defend their metal-on-metal hip replacements. Facing thousands of lawsuits, the makers of ...

Read More

Warning for Medtronic InterStim Neurostimulation Devices

Australian Health Agency Issues Warning for Battery Problem with Medtronic InterStim Neurostimulation Devices

Warning for Medtronic InterStim Neurostimulation DevicesTGA has issued a safety warning for InterStim and InterStim II neurostimulation devices, because of possible early depletion of the battery.

Read More

National Law Firms Calls for More FDA Action on Actos Bladder Cancer Threat

A national law firm is not satisfied with the way the U.S. Food & Drug Administration (FDA) has handled warnings regarding Actos (pioglitazone) bladder cancer risks. In a statement published today, Parker Waichman LLP called on the FDA to compel Takeda Pharmaceuticals, the maker of the type 2 diabetes drug, ...

Read More

Endo Agrees to Additional $775M Settlement for a Total of $2.6B

As of August 7, 2017, Endo International has agreed to set aside an additional $775 million to resolve the company’s remaining mesh lawsuits’ allegations related to the Transvaginal Mesh (TVM) Multidistrict (MDL) Litigation pending in the U.S. district Court of … Continue reading

Posted in Defective Medical Devices, Defective Products, Health Concerns, Product Recalls, Recalled Vehicles, Transvaginal mesh |

Johnson & Johnson Loses Fourth Transvaginal Mesh Trial

On May 26, 2017, health care giant Johnson & Johnson lost its fourth surgical mesh lawsuit when a Philadelphia jury returned a verdict of $2.16 million against Johnson & Johnson and its Ethicon Women’s Health and Urology division. Observers see … Continue reading

Posted in Defective Medical Devices, Transvaginal mesh |

Atrium C-Qur Hernia Mesh Complications and Lawsuits

Atrium C-Qur Hernia Mesh Complications and Lawsuits

A woman recently filed a lawsuit against Atrium Medical, the manufacturers of the Atrium C-Qur hernia mesh, alleging severe pain and injury after the mesh was used during an open repair of her ventral (abdominal) hernia in 2011. According to … Continue reading

Posted in Defective Medical Devices, Transvaginal mesh | Tagged , , , , |

C.R. Bard Recalls Halo One Guiding Sheath

The FDA Deems Halo One Guiding Sheath Recall a Class I The U.S. Food and Drug Administration (FDA) recently announced a Class 1 recall of C.R. Bard Peripheral Vascular Inc.’s Halo One thin-walled guiding sheaths over issues involving sheath separation, … Continue reading

Posted in Bard IVC Filter Injuries, Defective Medical Devices, Transvaginal mesh |

Boston Scientific Plaintiff Wins Appeal, Gets New Trial

Boston Scientific Plaintiff Wins Appeal, Gets New Trial

A woman who lost her case in the Boston Scientific transvaginal mesh litigation more than two years ago is getting another opportunity in court. Previously, she filed a lawsuit alleging that she suffered injuries caused by the Pinnacle Pelvic Floor … Continue reading

Posted in Defective Medical Devices, Transvaginal mesh | Tagged , , , , , , |

Illinois Woman Alleges Essure Complications Led to Removal of Uterus, Fallopian Tubes

Essure Issues Led to Removal of Uterus, Fallopian Tubes

Another lawsuit has been filed against Bayer over Essure, the permanent birth control device for women. An Illinois woman alleges that Essure implantation led to serious complications, ultimately leading to the removal of her uterus and fallopian tubes. Essure consists … Continue reading

Posted in Defective Medical Devices, Transvaginal mesh | Tagged , , , , , , , |

Vaginal Mesh Associated with Inflammation Revealed in New Study

Vaginal Mesh Linked with Inflammation Revealed in New Study

Surgical vaginal mesh is used in the treatment of pelvic organ prolapse (POP) and stress urinary incontinence in women. The University of Pittsburgh has revealed a significant connection between vaginal mesh and inflammation in patients. POP, common in older women, … Continue reading

Posted in Defective Medical Devices, Health Concerns, Transvaginal mesh | Tagged , , , , , , , |

J&J Used Deceptive Marketing for Transvaginal Mesh, Kentucky AG Alleges in Civil Suit

J&J Used Deceptive Marketing for Transvaginal Mesh

Johnson & Johnson and its medical unit Ethicon are once again facing allegations of deceptive marketing over its transvaginal mesh. Kentucky Attorney General Andy Beshear filed a lawsuit in Franklin Circuit Court under the Kentucky Consumer Protection Act, alleging the … Continue reading

Posted in Defective Medical Devices, Transvaginal mesh | Tagged , , , , , , |

Kentucky Attorney General Files Lawsuit Against Johnson & Johnson Over Transvaginal Mesh

KY ATTY GEN Lawsuit Against J&J Over Transvaginal Mesh

Kentucky Attorney General Andy Beshear announced on August 16, 2016 that his office was filing a civil lawsuit against Johnson & Johnson and its medical device unit, Ethicon, over surgical mesh devices used in gynecological surgery. The lawsuit alleges the … Continue reading

Posted in Defective Medical Devices, Transvaginal mesh | Tagged , , , , , |

FDA Approval of Transvaginal Mesh is Questioned by Victims

FDA Approval of Transvaginal Mesh is Questioned by Victims

A study by Northwestern University, published May 4, 2016 in Obstetrics and Gynecology criticized the U.S. Food and Drug Administation (FDA) for approving a number of high-risk health devices based on unsubstantiated clinical studies, including transvaginal mesh. Dr. Steve Xu, … Continue reading

Posted in Defective Medical Devices, Defective Products, Transvaginal mesh | Tagged , , , , , , , , , , , , , , |

© 2005-2017 Parker Waichman LLP ®. All Rights Reserved.