Because Bard Avaulta mesh has been linked to a number of different complications, patients implanted with the surgical mesh device may require one or more corrective measures. Necessary Bard Avaulta mesh corrective measures may include:
- IV therapy
- Blood transfusions
- Drainage of hematomas or abscesses
- Additional surgical procedures (i.e. doctors may need to remove the Bard Avaulta mesh)
The Food and Drug Administration (“FDA”) has not yet determined whether specific characteristics put some patients at an increased risk for Bard Avaulta mesh complications. Factors contributing to the need for Bard Avaulta mesh corrective measures may include the patient’s overall health, the surgical mesh material, the size and shape of the Bard Avaulta mesh, the surgical technique used, concomitant procedures undertaken (e.g. hysterectomy), and possibly estrogen status.
Avoiding the Need for Corrective Measures
To help avoid the need for Bard Avaulta mesh corrective measures, the
Related Topics
- Bard Avaulta Mesh Side Effects
- Avaulta Biosynthetic & Avaulta Plus Biosynthetic Support Systems
- Bard Avaulta Mesh Lawyer Lawsuit
- Bard Transvaginal Mesh Recall
- Cystocele &Transvaginal Mesh
- Bard Avaulta Mesh & Dyspareunia
- Transvaginal Mesh Infection
- Bard Avaulta Mesh Erosion
- Bard Avaulta Mesh Pelvic Organ Prolapse
- Bard Avaulta Mesh Stress Urinary Incontinence
- Transvaginal Mesh & Vaginal Prolapse
Dangerous Product Alerts
Similar Defective Devices
- Obtain specialized training for each mesh placement technique, and be aware of its risks.
- Be vigilant for potential adverse events from the mesh, especially erosion and infection.
- Watch for complications associated with the tools used in transvaginal placement, especially bowel, bladder and blood vessel perforations.
- Inform patients that implantation of surgical mesh is permanent, and that some complications associated with the implanted mesh may require additional surgery that may or may not correct the complication.
- Inform patients about the potential for serious complications and their effect on quality of life, including pain during sexual intercourse, scarring, and narrowing of the vaginal wall (in POP repair).
- Provide patients with a written copy of the patient labeling from the surgical mesh manufacturer, if available.
Bard Avaulta Legal Help for Those Who Need Corrective Measures
If you or a loved one required corrective measures to treat a Bard Avaulta mesh complication, such as infection, pain, or recurrence of prolapse and/or incontinence, you may be entitled to compensation for your injuries and should contact an attorney as soon as possible.
Contact a Bard Avaulta Lawyer Today
Contact our law firm today for a confidential and free case evaluation by our Bard Avaulta mesh injury lawyers. Attorney Felecia Stern can be reached confidentially at (877) 779-1414 (ext 211) or at stern@bernlieb.com.
