This is what patients feel when parts part with other parts:
• Instability in the knee when standing or putting weight on it;
• backwards or sideways motion of the knee;
• decreased range of motion;
• inflammation, swelling, heat; and
• constant throbbing pain.
This is what DePuy Attune knee replacement patients report.
The Journal of Knee Surgery has identified an unusually high rate of premature failure in DePuy Attune Synthes knee replacements. A review of the FDA’s Manufacturer and User Facility Device Experience (MAUDE) database revealed 21 reports of tibial loosening at the implant–cement interface in just the two months prior to the journal’s report.
When they removed the defective device, some surgeons have reported that they saw no evidence that cement or bone had ever adhered to the implant. Others described the removed metal tibial insert as clean from any bond—essentially looking the same as it did when it was removed from the sterile packaging and implanted.
It was clean; it never stuck; the cement failed. What caused the glue to fail is still not entirely clear, but patients were hurt.
DePuy Synthes is no stranger to controversy concerning its Attune knee replacements. In June 2015, the FDA recalled its Tibial Articulation Surface Instrument, a device used during knee replacement surgery to ensure correct placement of the tibia. A small coil that was part of the instrument could become detached and be left inside a patient. It’s the modern equivalent of a sponge left behind when the incision is closed.
READ MORE DEPUY SYNTHES ATTUNE KNEE REPLACEMENT LEGAL NEWS
Nonetheless, Johnson & Johnson, DePuy Orthoopaedics and DePuy Synthes continue to be market-makers. No recalls of the DePuy Synthes Attune knee replacement device have been issued yet and no lawsuits have been filed to date. The situation seems increasingly ripe for both.