Our lawyers are reviewing potential lawsuits for people who were injured after undergoing hip replacement surgery with Stryker LFIT V40 femoral heads. These devices have been associated with a large number of complaints involving taper lock failure, which can require the need for extensive and painful hip revision surgery.
Free Confidential Lawsuit Evaluation: If you or a loved one suffered complications after hip implant surgery, you should contact our law firm immediately. You may be entitled to compensation by filing a suit against the manufacturer and our lawyers can help.
Update: Federal Stryker LFIT V40 Lawsuits May Be Consolidated into MDL
February 23, 2017 – Plaintiffs’ lawyers have requested multidistrict litigation (MDL) status for lawsuits involving the Stryker LFIT Anatomic Cobalt Chromium V40 Femoral Head. They are recommending the District of Massachusetts for the MDL because it provides an easily accessible location, the venue can handle a high volume of cases, and it has very experienced judges.
What’s the Problem?
The Stryker Corporation has notified Australia’s Therapeutic Goods Administration (TGA) of potential safety concerns linked to the LFIT Anatomic CoCr V40 femoral head attributed to a “possible taper lock interface inconsistency.” This problem may result in a number of hip implant complications including:
- Dissociation of the femoral head from the hip stem;
- Breakage of the hip stem trunnion;
- Metallic debris in the soft tissue surrounding the implant, which can lead to bone and tissue necrosis;
- Insufficient soft tissue tension;
- Noises emanating from the hip implant;
- Decrease in the strength of the bone fixation, and
- Increased wear debris from the components of the hip replacement device.
Which Products are Affected?
The following modular hip implants were specifically noted in the Australian safety alert:
Catalog Number Head Diameter Offset
6260-9-236 36mm +5
6260-9-240 40mm +4
6260-9-244 44mm +4
6260-9-340 40mm +8
6260·9-440 40mm +12
6260-9-344 44mm +8
6260-9-444 44mm +12
Has the FDA Issued a Warning?
To date, no similar notification has been issued by the U.S. Food & Drug Administration (FDA). The hazard alert issued in Australia is not a product recall; however, it is nevertheless a serious issue that patients and their orthopedic surgeons need to be aware of, especially considering the well-documented risks of metallosis and dissociation of modular hip implants. It is unknown whether the FDA will issue similar warnings or require Stryker to issue a recall for the LFIT V40 femoral head.
Stryker Hip Recalls
This is not the first time Stryker has had problems with its hip replacement devices. In July 2012, the company recalled the Rejuvenate and ABG II hip implants over concerns the devices may corrode, fret and fail within a few years after being implanted. Complications associated with the devices included:
- difficulty walking
- squeaky joints
- faulty components
- plant contamination
- local tissue damage
- high failure rates
Has a Class Action Been Filed?
In 2014, a number of lawsuits were filed on behalf of patients who suffered complications after being implanted with Stryker Accolade TMZF hip stems and LFIT anatomic V40 femoral heads. These complaints, which alleged that the devices’ components were defectively designed and manufactured, were individually filed and not part of a class action.
It is not anticipated that a class action lawsuit will be filed over injuries alleged from Stryker LFIT V40 femoral heads. However, our lawyers are reviewing potential individual lawsuits on behalf of injured parties. If we determine that you have a valid claim, you may be eligible to receive compensation for medical expenses, lost wages, pain and suffering, and other damages.
Alaska Couple Files Stryker LFIT V40 Lawsuit
February 15, 2017 – A couple from Alaska has filed a products liability lawsuit against Stryker Corp. over injuries alleged from the LFIT V40 hip implant. According to the lawsuit, problems with the Accolade TMZF femoral stem and LFIT V40 Head forced the Plaintiff to undergo painful hip revision surgery, during which the surgeons found multiple complications associated with the components.
Lawyers Request MCL for Stryker LFIT Litigation
February 13, 2017 – Plaintiffs lawyers are seeking multicounty litigation (MCL) status in New Jersey for lawsuits alleging injuries from the Stryker LFIT Anatomic Cobalt Chromium V40 Femoral Head. The proposed venue for the litigation is Bergen County, where at least 25 cases are currently pending. Court records indicate that filings have recently increased, with at least 85 cases filed in courts across the U.S.
Do I Have a Stryker LFIT Lawsuit?
The Medical Device Litigation Group at our law firm is an experienced team of trial lawyers that focus on the representation of plaintiffs in Stryker LFIT lawsuits. We are handling individual litigation nationwide and currently accepting new injury cases in all 50 states.
Free Case Evaluation: Again, if you were injured or suffered damages from a Stryker hip replacement device, you should contact our law firm immediately. You may be entitled to a settlement by filing a suit and we can help.