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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
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    • Video Library
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Home » Stryker Recalls LFIT Hip Implants Over Device Failure Issues

Stryker Recalls LFIT Hip Implants Over Device Failure Issues

Stryker Corporation has issued a voluntary recall of its LFIT Anatomic CoCr V40 hip replacement devices. The company sent an urgent recall notification to surgeons late August 2016 advising of potential hazards associated with these devices. Specifically Stryker is recalling LFIT Anatomic CoCr V40TM Femoral Heads manufactured prior to 2011. The following chart shows additional identifying information for this recall.

Catalog NumberHead DiameterOffset
6260-9-23636mm5
6260-9-24040mm4
6260-9-24444mm4
6260-9-34040mm8
6260-9-44040mm12
6260-9-34444mm8
6260-9-44444mm12

 

Patients are at risk for suffering loss of mobility, dislocation, severe inflammation, severe pain, fracture and other injuries. Stryker warns these implants may give off excessive metallic debris, fracture at the hip stem trunnion, lose bone fixation strength, and disassociate the femoral head from the hip stem causing serious injury to patients.

If you or someone you know has a Stryker LFIT hip implant and has suffered serious injury, contact us. Our product liability attorneys have litigated claims against medical device manufacturers and can advise you of your legal rights and options.

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