Press Releases
03/24/2021
Attorney General Tong Announces $188.6 Million Multistate Settlement with Medical Device Manufacturer Boston Scientific Corporation
(Hartford, CT) -- Attorney General William Tong and Consumer Protection Commissioner Michelle H. Seagull today announced a multistate settlement with Boston Scientific Corporation (Boston) to resolve allegations of deceptive marketing of its surgical mesh products for women. The settlement requires Boston to pay $188.6 million to 47 states and the District of Columbia to resolve allegations that it deceptively marketed transvaginal surgical mesh devices to patients. Connecticut’s share of the settlement is $1,811,069.
“Boston Scientific misled millions of women through deceptive marketing that disguised the dangers of surgical mesh. Thousands of women suffered serious complications as a result. In addition to an $188.6 million fine, this settlement forces Boston Scientific to undertake serious marketing, training, and clinical trial reforms to ensure this type of preventable and unacceptable tragedy never happens again,” said Attorney General Tong.
“This case is another example of the serious consequences deceptive advertising can have on consumers,” said Consumer Protection Commissioner Michelle H. Seagull. “The terms of this settlement are an important step toward protecting women from further harm due to the poor marketing and misrepresentation of the risks associated with surgical mesh by Boston Scientific.”
Surgical mesh is a synthetic woven fabric that is implanted in the pelvic floor through the vagina to treat common health conditions in women such as stress urinary incontinence and pelvic organ prolapse. These are common conditions faced by women due to a weakening in their pelvic floor muscles caused by childbirth, age, or other factors. Although use of surgical mesh involves the risk of serious complications and is not proven to be any more effective than traditional tissue repair, millions of women were implanted with the devices and thousands of women are alleged to have suffered serious complications resulting from these devices.
The complaint alleges that Boston misrepresented the safety of these products by failing to disclose the full range of potential serious and irreversible complications caused by mesh, including chronic pain, voiding dysfunction, and new onset of incontinence.
The settlement provides comprehensive injunctive relief. Under the terms of the settlement, Boston is required to:
Marketing Reforms:
• For marketing materials intended for consumers, describe complications in understandable terms;
• For certain marketing materials, disclose significant complications, including the inherent risks of mesh;
• Refrain from representing that any inherent risks of mesh are risks common to any pelvic floor or other surgery not involving mesh;
• Refrain from representing that inherent mesh complications can be eliminated with surgical experience or technique;
• Refrain from representing that surgical mesh does not cause a foreign body reaction;
• Refrain from representing that surgical mesh remains soft, supple, or pliable after mesh is implanted inside the body;
• Refrain from representing that surgical mesh does not potentiate infection or does not increase the likelihood of infection;
• Refrain from representing that surgical mesh repair is superior to native tissue repair unless such representations are supported by valid scientific evidence;
Training Reforms:
• Inform healthcare providers of significant complications when providing training regarding procedures for insertion and implantation;
• Maintain policies requiring that its independent contractors, agents, and employees who sell, market, or promote mesh are adequately trained to report patient complaints and adverse events to the company;
Clinical Trial Reforms:
• When submitting a clinical study or clinical data regarding mesh for publication, disclose the company’s role as a sponsor and any author’s potential conflict of interest;
• Refrain from citing any clinical study, clinical data, preclinical data, research, or article regarding mesh for which the company has not complied with the disclosure requirements in the injunction;
• Include a sponsorship disclosure provision requiring consultants to contractually agree to disclose in any public presentation or submission for publication any sponsorships by Boston related to the contracted-for activity;
• Register all Boston-sponsored clinical studies regarding mesh with ClinicalTrials.gov.
The investigation that resulted in today’s settlement was led by California and Washington along with Florida, Indiana, Maryland, Ohio, South Carolina, and Texas. Joining this multistate settlement are Alabama, Alaska, Arizona, Arkansas, Colorado, Connecticut, Delaware, Georgia, Hawaii, Idaho, Illinois, Iowa, Kansas, Kentucky, Louisiana, Maine, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Oklahoma, Pennsylvania, Rhode Island, South Dakota, Tennessee, Utah, Vermont, Virginia, Wisconsin, and the District of Columbia.
A copy of the complaint is here and the stipulated judgment submitted for court approval is here.
Assistant Attorney General Brendan Flynn and Michael Wertheimer, Deputy Associate Attorney General & Chief of the Consumer Protection Section assisted the Attorney General in this matter.
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Media Contact:
Elizabeth Benton
elizabeth.benton@ct.gov
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