Smith and Nephew Hip Recall

Smith & Nephew PLC announced a recall of 185 hip replacement implants after patients were forced to have surgery to replace improperly fitted devices. The recall was due to mislabeled products, causing a mismatch between implant pieces. Smith & Nephew failed to meet post-marketing surveillance and reporting requirements designed to make sure that the hip replacement system was safe and effective.

Goldenberg Heller & Antognoli has provided comprehensive legal advice to protect our clients for more than 30 years. Our attorneys handle all Smith & Nephew Hip Recall liability cases on a contingency fee basis, and we offer free initial consultations. You pay nothing for our services unless we obtain a settlement or an award on your behalf.

Issues Connected to Smith and Nephew Hip Recall Claims

Smith & Nephew’s defective implants have been linked to several serious issues including:

  • Bone fractures
  • Implant loosening or dislocation
  • Metallosis
  • Infection

FDA Warning to Smith & Nephew

The FDA issued a warning to Smith & Nephew about quality control problems at their German hip replacement implant facility in 2010, which is responsible for the manufacturing of the R3 Ceramic Acetabular System. Inspectors stated Smith & Nephew failed to provide proper corrective actions in maintaining procedures to ensure the quality and safety of their products. If you have received a hip implant from Smith & Nephew, we’re here to review your case and determine the proper next steps.

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Free Smith and Nephew Hip Recall Claims Consultation

We assist clients in winning the compensation they deserve throughout St. Louis and the Metro East area in both Illinois and Missouri. We’re ready to discuss your specific legal needs.

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2017

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