Medical Device Injury

Nearly 3,800 Blood Clot Filter Lawsuits Filed Against Product Manufacturers

A total of 3,769 blood clot filter lawsuits have been filed against Cook Medical, Inc. and C.R. Bard, Inc. alleging that the retrievable IVC filters manufactured by the companies have caused plaintiffs to suffer from severe complications. Two IVC filters are named in the Cook Medical litigation: the Gunther Tulip and Cook Celect IVC blood

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Lawsuit: Hernia Mesh Failure Led to Bowel Resection, Removal Surgery

A South Florida woman who claims she suffered severe complications caused by a hernia mesh is suing the manufacturer, accusing the company of a host of charges including liability, breach of warranty, negligence, and fraud. Deborah T. filed her hernia mesh lawsuit against Atrium Medical Corporation on July 21, 2017, in New Hampshire federal court.

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Hernia Mesh Infection Led to Additional Surgeries: Lawsuit

A Texas woman who allegedly suffered a hernia mesh infection has filed a lawsuit against Ethicon Inc. and Johnson & Johnson, claiming the medical device was defective. Plaintiff Lydia E. alleges she was implanted with two Physiomesh hernia mesh devices on Jan. 7, 2013 to repair a hernia. On Feb. 10, 2014, she underwent surgery

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Study: IVC Filter Side Effects Increase the Longer Device in Body

A new study finds that IVC filters may pose increased health risks the longer the devices remain in the body. According to a study by the American Heart Association, a period of seven months or more is the threshold for a greater risk of failure during a retrieval procedure. The IVC filter study was published

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Defective Hernia Mesh Leads to Multiple Surgeries: Physiomesh Lawsuit

A Florida couple has filed a Physiomesh lawsuit against Johnson & Johnson and Ethicon claiming that the hernia mesh used in the wife’s surgery was defective and unsafe. Plaintiffs Sheri J. and Alfred J. claim in this Physiomesh lawsuit that Sheri suffered multiple complications after her hernia surgery using Ethicon’s Physiomesh hernia mesh device. In

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Complications Requiring Hernia Mesh Revision Surgery Prompt Lawsuit

A product liability lawsuit has been filed against Ethicon and parent company Johnson & Johnson alleging that a man’s hernia repair using Ethicon Physiomesh led him to develop complications ultimately requiring hernia mesh revision surgery. Plaintiff Larry S. filed his lawsuit in South Carolina federal court after his surgical mesh became infected. In his initial

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August 11 Marks Date to Consider Class Certification in IVC Filter Litigation

On August 11, 2017, U.S. District Judge David G. Campbell will be hearing oral arguments in Arizona federal court to decide if class certification will be established for IVC filter plaintiffs. The proposed class action lawsuit seeks medical monitoring services for plaintiffs who were implanted with an IVC filter and who are seeking to avoid

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