Stryker LFIT V40 Recall

The Stryker LFIT V40 hip replacement lawsuit involves the LFIT Anatomic V40 femoral heads utilized with the Stryker Accolade, Citation, Meridian, Exeter, Reliance, Definition, and Restoration TMZF titanium stems.

The LFIT heads manufactured before 2012 are experiencing a high failure rate, and the company issued a voluntary recall in August. The defect can result in cobalt and poisoning, spontaneous disassociation, femur fracture, soft tissue necrosis, muscle damage, bone loss, and revision surgery.

Stryker LFIT V40 Femoral Heads Subject to Recall:

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Contact our hip replacement lawyers to review whether you or a loved one may be entitled to financial compensation. Levy Konigsberg LLP is currently accepting hip replacement injury cases in all 50 states.

If you or a loved one suffered a serious injury after having a hip replacement, you may be entitled to a cash award and compensation for medical expenses. For a free confidential consultation with lawyers at our law firm, please call 1-866-992-5279 or submit an email inquiry above.