LPS Lower Extremity Dovetail Device Recalled By DePuy Over Safety Risk
DePuy Orthopaedics has announced the recall of LPS Lower Extremity Dovetail Intercalary Components because of an issue that could lead to pain or even a revision procedure. The device, which is implanted in patients requiring a partial or total femur replacement or a proximal tibia replacement, can experience a fracture along the female portion of the device. It reportedly does not take extensive activity and pressure for this to occur; the fracture can take place even during simple walking. When it happens, the user can experience intense pain, lost limb function, an infection, and more, and the failure may necessitate a revision surgery. Surgeons are being asked to cease implanting the device and doctors are being asked to speak with patients who have gotten the devices implanted.
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