Did you know that one out of every 30 women with a vaginal sling implanted for urinary incontinence, a revision surgery is required within 10 years or so? Isn’t that scary? As per surveys, around 61 mesh devices in the market never underwent a clinical trial. Can you relate with self? Read on.
Are you implanted with transvaginal mesh? Do you face complications that can be root caused by this implant? Do you want to know if you are eligible for filing transvaginal mesh lawsuits?
To begin with, any mesh device that has been approved by the FDA but couldn’t abide by the promises it made, or couldn’t provide enough warnings of the possible adverse effects, are entitled for a lawsuit. Additionally, there are several mesh manufacturers that have not withdrawn their devices despite the warnings sent from the FDA.
Bans and limitations of mesh products:
As reported in January 2018, three countries have issued market bans on these mesh devices. Australia was the first to take action, though New Zealand is currently the only country to issue a complete ban on these products for gynecological uses.
Though the FDA has not yet taken any step against these as of now, the warnings have been tightened back in 2011.
Do you qualify to file a lawsuit?
If you are experiencing any of the following symptoms, you might qualify to join an active case:
A transvaginal mesh lawsuit will likely be for defective products. However, it falls under medical malpractice, if the surgeon implanted it incorrectly. A transvaginal mesh implant that did not work the way it was intended could fall into one of three categories for defective products, or possibly even more than one:
Under these circumstances, a victim is eligible to file transvaginal mesh lawsuits against the device manufacturer. If you are one of those victims, get in touch with Transvaginal Mesh Lawsuit Update on https://transvaginalmeshlawsuitupdate.com or at 1(855)631-1517 for details.