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Stryker LFIT V40 Lawsuit Overview
An Alaskan duo has initiated a legal action on product liability grounds against Stryker Corp., attributing their injuries to the LFIT V40 hip implant. The primary allegations against Stryker include defective design that makes the implant prone to fretting, corrosion, and failure, leading to complications such as elevated metal ion levels, pseudotumors, and the need for revision surgeries.
The lawsuit seeks damages in excess of $75,000 for injuries caused by the defective hip implant components. Stryker recalled certain sizes of the LFIT V40™ femoral head in August 2016 after receiving numerous complaints of taper lock failure.
Latest Stryker LFIT V40 Lawsuit Updates
- March 2017 – According to court documents, a patient who received an Accolade TMZF femoral stem with an LFIT V40 Head during hip replacement surgery in March 2008 developed elevated blood cobalt levels, indicating implant fretting and corrosion [1]. Subsequent MRI scans revealed large soft tissue masses, and the patient required revision surgery in January 2015, where surgeons found chronic inflammation, adverse tissue reactions, corrosion, and trunnionosis.
- August 2016 – Stryker recalled certain sizes of the LFIT V40™ femoral head after receiving a large number of complaints regarding taper lock failure [2]. Unfortunately, this action came too late for many patients who had already experienced complications from the defective implants.
Stryker LFIT V40 Injuries & Side Effects
Patients who received the Stryker LFIT V40 hip implant have reported a range of serious complications and injuries.
The following serious side effects have been documented:
- Metal Ion Poisoning: Elevated cobalt and chromium levels in blood due to metal component wear
- Pseudotumors: Formation of fluid-filled masses and soft tissue reactions around the implant
- Trunnionosis: Corrosion and wear at the head-neck junction of the implant
- Chronic Inflammation: Persistent inflammatory responses in joint tissues
- Implant Failure: Complete breakdown requiring revision surgery
Do You Qualify for a Stryker LFIT V40 Lawsuit?
You may qualify for a Stryker LFIT V40 lawsuit if:
- You received a Stryker LFIT V40 hip implant between 2008-2016
- You experienced serious side effects including elevated metal ion levels, pseudotumors, chronic pain, or implant failure
- The injuries required medical treatment, revision surgery, or hospitalization
- You can provide medical documentation linking your injuries to the Stryker LFIT V40 implant
Evidence Required for a Stryker LFIT V40 Lawsuit
Essential evidence includes medical records detailing your implant surgery and complications, records of revision surgeries, documented symptoms, and expert testimony linking the device to your health issues. Blood test results showing elevated metal ion levels and imaging studies revealing pseudotumors or other complications are particularly important for strengthening your case.
Damages You Can Recover
If successful in your Stryker LFIT V40 lawsuit, you may be entitled to compensation for:
- Medical expenses related to complications and revision surgeries
- Lost wages due to time away from work
- Pain and suffering caused by the defective implant
- Punitive damages against the manufacturer
Stryker LFIT V40 Recall Information
In August 2016, Stryker recalled certain sizes of the LFIT V40™ femoral head after receiving a large number of complaints of taper lock failure [3]. This recall highlighted known issues with the implant that led to patient complications.
FAQs
1. What Evidence Is Essential For Supporting My Hip Implant Lawsuit?
Essential evidence includes medical records detailing your implant surgery and complications, records of revision surgeries, documented symptoms, and expert testimony linking the device to your health issues.
2. Can I File A Lawsuit If My Hip Implant Was Recalled?
Yes, if your Stryker LFIT V40 hip implant was recalled and you experienced complications, you may be eligible to file a lawsuit. The recall strengthens your case by highlighting known issues with the device.
3. Are There Class Action Lawsuits For Stryker LFIT V40 Hip Implants?
Yes, there are class action lawsuits and MDL cases for Stryker LFIT V40 hip implants, including MDL No. 2768 in Massachusetts and a consolidation in New Jersey. These cases address claims of device failure and health complications.
Get A Free Stryker LFIT V40 Recall Evaluation With Our Lawyers
Time is limited to pursue legal action against Stryker for LFIT V40 hip implant injuries. Statutes of limitations vary by state but typically allow only 2-3 years from the date of injury or discovery of harm to file a lawsuit.
Our legal services include:
- Free, confidential consultations to evaluate your case
- No upfront costs or fees required
- Payment only if we win your case and secure compensation
Related Articles:
- Stryker Hip Litigation Approaches 400 Cases
- Stryker LFIT Class Action Lawsuit
- Stryker LFIT V40 Lawsuits may be Consolidated into MDL
Check out our website to find out which medical device lawsuits our lawyers are currently accepting.
References:
- https://topclassactions.com/lawsuit-settlements/lawsuit-news/stryker-accolade-hip-stem-failure-caused-design-flaws-couple-claims/
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=149782
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=149782