If your Zimmer knee device fails you will most likely
require revision surgery which is much more evasive and complicated than the initial knee replacement surgery.
The FDA stated that the use of a Transvaginal mesh implant like the Bard Avaulta, Johnson & Johnson, American Medical Systems, Boston Scientific, and other vaginal mesh is no more effective compared to other surgeries yet is much more likely to cause injury and
require revision surgery.
Or when a second doctor tells you that
you require revision surgery?
If you have been told that
you require revision surgery, contact The Gomez Law Firm today to protect your legal rights.
Only five per cent of patients
require revision surgery over a 10 - year period.
If you or a loved one have been injured or
required revision surgery for a defective hip implant, let us know.
In 2010, reports disclosed that approximately 9 % of people with the Zimmer NexGen CR - Flex Porous Femoral component knee replacement
required a revision surgery within two years.
Studies began to link these metal hip devices to serious injuries in patients around the world — even injuries that were debilitating or
required revision surgery.
Transvaginal mesh has been found to fail at a high rate, often leading to tissue damage, internal bleeding, and severe pain
requiring revision surgery.
Not exact matches
Consumers have reported side effects of the BioMet hip replacements such as severe pain, swelling and difficulty walking, and many have
required hip
revision surgery.
Revision surgery is often
required to fix vaginal mesh defects and this too can lead to more pain and complications.
Revision Surgery To remedy transvaginal mesh complications and injuries, revision surgery may be required, which also could lead to possible complications and addition
Revision Surgery To remedy transvaginal mesh complications and injuries, revision surgery may be required, which also could lead to possible complications and additiona
Surgery To remedy transvaginal mesh complications and injuries,
revision surgery may be required, which also could lead to possible complications and addition
revision surgery may be required, which also could lead to possible complications and additiona
surgery may be
required, which also could lead to possible complications and additional pain.
The Gynecare Prolift is the subject of the first transvaginal mesh lawsuit to go to trial in New Jersey, where Linda Gross alleges the device failed and
required 18
revision surgeries.
As with any kind of
surgery, there are risks involved and, in certain circumstances, more than one
revision procedure may be
required.
Revision surgery can be
required to remove or replace a mesh implant - especially if it has eroded into the urethra, bladder, or vaginal walls.