DePuy Attune Knee Implant Failures Continue

Patients who’ve received a DePuy Synthes Attune leg replacement have observed an unusually higher rate of early inability of the tibia element. Many experts say that estimation is significantly to low since it does not consider unreported occasions.

An in depth at look the FDA’s Supplier and User Center Device Experience (MAUDE) databases shows a large number of information of tibia loosening at the implant-cement program.

Patients have gone back with their doctors complaining of bloating, pain and lowered flexibility and been required to undergo agonizing revision surgery to displace the defective leg implant. You can
browse http://www.depuykneelawsuit.com/depuy-knee-recalls.aspx to know more about the DePuy attune knee lawsuit.

During revision surgeries, cosmetic surgeons continue to face tibia loosening. They believe the Attune leg replacement is susceptible to loosening because it’s simple surfaces never let medical glue to add the components appropriately to the knee bones. Quite simply, because the top of device is so simple, the glue doesn’t keep.

DePuy Synthes, a subsidiary of Johnson & Johnson, has rejected claims that these devices are faulty. No stranger to lawsuits and product remember – DePuy was in charge of the major medical device inability settlement ever sold regarding its ASR hip alternative joint – the business is facing new rounds of litigation from patients who experienced after having Attune leg replacements.