Sentences with phrase «transvaginal mesh surgery after»
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Women who have experienced serious side effects after undergoing transvaginal mesh surgery can consult our drug injury lawyers for free legal advice.
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Many transvaginal mesh manufacturers such as Johnson & Johnson and C. R. Bard have stopped selling their mesh devices after thousands of women have complained of severe pain, limited mobility and the need for revision surgery.
Several manufacturers have issued transvaginal mesh recalls after studies linked the devices to severe complications and potential need for revision surgery.
The FDA issued a mesh warning after receiving an influx of complaints from patients who allege that their transvaginal mesh device were causing severe complications, pain and sometimes revision surgery.
If you or a loved one has suffered complications from transvaginal mesh after POP or SUI repair surgery, you may be eligible to file a lawsuit.
The most common side effect reported by patients with transvaginal mesh was vaginal mesh erosion, or exposure of the mesh patch after surgery.
More than 600 patients who developed complications after surgery have filed transvaginal mesh lawsuits against manufacturers of the patch.
Patients who experience pain or other problems with transvaginal mesh may be forced to undergo repair surgery in order to correct problems that occurred after the mesh implantation.