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Google Reviews Logo

317.636.6481

One Indiana Square, Suite 1400 Indianapolis, Indiana 46204

Make a Payment
  • Home
  • Firm Overview
  • Our Attorneys
  • Practice Areas
    • Pharmaceutical Drug & Medical Device Litigation
    • Personal Injury
    • Sexual Abuse
    • Class Action
    • Medical Malpractice
    • Eminent Domain
    • Family Law
    • Business Services, Real Estate & Business Litigation
    • Bankruptcy, Creditor’s Rights, & Commercial & Business Law
    • Appellate Law
  • Firm News
    • News & Announcements
    • Alerts
  • Resources
    • Video Library
    • Blog
  • Contact Us

Home » FDA Recalls Zimmer Hip Implants M/L Taper with Kinectiv Technology Prosthesis

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.

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