FDA Recalls Zimmer Hip Implants M/L Taper with Kinectiv Technology Prosthesis
The FDA issued a recall for the Zimmer M/L Taper with Kinectiv Technology Femoral Stems and Necks hip implants on June 19, 2015. Patients are at an increased risk for allergic reactions, pain, infections, or death related to high level of manufacturing residue on these implant components. The FDA states that revision surgery to replace the defective implants may be necessary.
If you or someone you know received a Zimmer M/L Taper with Kinectiv Technology prosthesis and has suffered from a serious injury, contact us. Our personal injury product liability attorneys can give you a free case evaluation and discuss your legal rights and options.
