Stryker LFIT V40 Hip Implant Lawsuits

Stryker LFIT V40 Hip Implant Lawsuits

Loncar Associates is now investigating Stryker LFIT V40 product defect lawsuits in order to ensure victims receive due compensation

While administration of a $1.4 billion dollar settlement for their defective, recalled stems (Rejuvinate and ABGII) winds down, Stryker finds itself at the center of another recall related to their cobalt/chromium femoral head – the LFIT V40.

At this time Stryker is only recalling certain, specific lots of the LFIT femoral head, all manufactured prior to 2012.  These recalled femoral heads were used as a part of the Accolade and Accolade 2 hip systems.  While not affected by the recall, the LFIT femoral head is also used with Stryker’s Meridian and Citation stems as well.

Whether the recall is due to a design defect or a problem in the manufacture process is unknown at this time and Stryker has not released any information beyond the recall itself.  The hips are being recalled due to early device failure resulting from damage where the femoral head meets the stem. Corrosion, metallosis, liner fracture, and stem fractures have all been associated with the recalled device.

Contact Loncar Associates today to participate in Stryker LFit V40 hip implant lawsuits

Recall notices are just being mailed out.  If you have received a recall notice call your orthopedist first.  Then contact Loncar Associates immediately for a confidential case evaluation from a law firm who has recently resolved hip cases with Stryker.  As attorneys, we are not qualified to provide you with medical care concerning your recalled hip.  Likewise, your orthopedist is simply not qualified to offer you legal advice regarding this matter.  This recall creates important legal deadlines that may impact your right to compensation.  Even if you have not yet developed problems with your recalled hip, act now.

Under the terms of our contingency fee contract, we are owed nothing unless we successfully resolve your case.  We can quickly identify your hip and review your legal options.  If you do not know what type of hip you have or if your LFIT is not part of the recall, contact my office immediately as we are investigating all LFIT devices for potential litigation. Loncar Associates is investigating cases in all 50 states. Contact Loncar Associates immediately for a free, confidential case evaluation using the form on the side or by calling toll free at 800.285.4878.

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