
Gynecare Mesh Withdrawn: Letter to the Court
The letter sent to the court notifying of Ethicon's decision to withdraw four Gynecare vaginal meshes from the market.
The letter sent to the court notifying of Ethicon's decision to withdraw four Gynecare vaginal meshes from the market.
Johnson & Johnson have stated that they will stop producing vaginal mesh products.
DePuy's compensation packets are not enough for clients facing large medical bills and medications.
Johnson & Johnson's vaginal mesh was on the market for three years, unapproved by the FDA.
Infographic depicting the 510(k) process the FDA used to approve transvaginal meshes for sale on the market.
Patients having problems with the DePuy reimbursement process may still be able to file a lawsuit to seek maximum compensation for their losses.
A vaginal mesh lawsuit against Johnson and Johnson has been filed alleging that the Gynecare mesh was defective and caused the plaintiff mesh erosion, pain and other side
A new study reveals that orthopedic surgeons are still receiving considerable payments from medical device manufacturers.
A Medtronic recall of the SynchroMed II Implantable Infusion Pump has been issued due to a battery flaw.
Due to the high number of reported vaginal mesh complications, the FDA is considered stricter regulations for those POP vaginal meshes.