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Disclaimer: The information provided on Exactech Lawsuit serves educational purposes only. Ethen Ostroff Law is no longer accepting new cases concerning Exactech as discussed here. This content offers general insights into legal matters and is not a replacement for professional legal advice. Individuals should consult qualified legal professionals for advice tailored to their specific situations.
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Product Liability

Exactech Lawsuit: Seeking Compensation for Premature Wear of Implants

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Medical replacement devices, like knee and hip implants, are crucial in improving mobility and enhancing the quality of life for those with severe joint issues. These devices, designed to last many years, enable patients to live active, pain-free lives. However, when they fail due to defects, the impact can be severe. Exactech recently issued recalls for certain knee, hip, and shoulder replacement devices found to have defects, causing them to wear out prematurely. The defect results in pain, limited mobility, and the need for additional surgeries. The recalls have affected thousands of patients. Consequently, numerous lawsuits have been filed against Exactech. Affected patients seek justice and compensation for their injuries and related costs. If you or a loved one has experienced issues with an Exactech knee or hip replacement, you might consider joining an Exactech lawsuit. Here, Ethen Ostroff Law provides essential information about the lawsuit and how we can help you.

Exactech Replacement Medical Devices

Exactech replacement medical devices are advanced implants designed to address joint issues, mainly knee and hip replacements. These devices have revolutionized orthopedic care by offering innovative solutions for various conditions.

  • Ankle replacements: Used for severe arthritis or joint degeneration when other treatments fail. These implants restore ankle mobility and function, reducing pain and improving stability. 
  • Hip replacements: Address hip joint deterioration from arthritis or injury. Durable implants improve mobility, reduce pain, and enhance hip stability. 
  • Knee replacements: Replace damaged or deteriorating knee joints, alleviating pain and stiffness from conditions like osteoarthritis. They help individuals regain mobility and quality of life. 
  • Shoulder replacements: Used for shoulder joint issues caused by arthritis, rotator cuff tears, or injuries. These implants restore range of motion and stability, improving daily activities and recreational pursuits.

Exactech's Orthopedic Solutions

Here are some of the key implants offered by Exactech:

Ankle replacement devices:

  • Vantage Total Ankle System 
  • Vantage PSI

Hip replacement devices:

  • Alteon 
  • Novation 
  • BIOLOXdelta 
  • AcuMatch 
  • MCS 
  • Connexion GXL

Knee replacement devices:

  • Arthrofocus 
  • Optetrak 
  • Optetrak Logic 
  • Truliant

Shoulder replacement device:

  • Equinoxe Shoulder System

These devices are carefully designed to address specific orthopedic needs, offering reliable solutions for joint-related conditions. Each implant is rigorously tested to ensure optimal performance and positive patient outcomes.

The Exactech Recall

Recently, concerns about the safety of certain Exactech implants led to a recall of various joint replacement devices, including knee, hip, shoulder, and ankle replacements. The issue was traced to defective packaging bags that lacked the necessary oxygen barrier layers. These defective bags allowed oxygen to reach the plastic (polyethylene) components before implantation, causing oxidation. This oxidation could lead to accelerated wear, fractures, and device failure over time. To ensure patient safety, Exactech took proactive steps to address this problem.

Exactech Devices with Defective Packaging

Exactech recalled around 657,391 joint replacement devices made between 2004 and August 2021. The FDA labeled this a Class II recall, meaning the devices might cause serious injury or temporary illness. The recalled devices include:

Types of Device Models Initial Recall Date And Number Recalled
Hip
Novation, AcuMatch, MCS
June 2021 , 39,942
Ankle
Vantage
August 2021 , 3,720
Knee
Optetrak Logic, Truliant, Arthrofocus
August 2021 , 489,498
Shoulder
Equinoxe Shoulder System
March 2024 , 124,231

Timeline of the Exactech Recalls Initiated to Date

  • June 2021: Exactech recalled its Novation, Acumatch, and MCS hip replacement devices due to “GXL” liners that could wear out prematurely. The FDA classified this as a Class II recall, indicating potential for temporary or reversible health issues. 
  • October 2021: Exactech recalled its Optetrak, Logic, and Truliant knee replacements and Vantage total ankle replacement devices. This was also a Class II recall. 
  • February 2022: Exactech expanded the recall for Optetrak, Logic, and Truliant knee replacements and Vantage total ankle replacements due to defective packaging. About 80% of these devices made since 2004 were affected. 
  • April 2022: Exactech issued a notice advising against implanting knee and ankle replacement devices shipped in defective packaging, covering those manufactured between January 2004 and August 2021. 
  • August 2022: Exactech expanded its hip replacement recall including all devices with polyethylene components in defective packaging. The FDA classified this as a Class II recall. 
  • March 23, 2023: The FDA reminded patients and healthcare providers about the recall of Exactech joint replacement devices made between 2004 and August 2021. 
  • June 2023: Exactech recalled its shoulder replacement devices due to issues with the devices and implantation tools, unrelated to packaging. This was also a Class II recall. 
  • January 2024: The FDA announced Exactech’s refusal to recall shoulder implant devices shipped in defective packaging, like earlier ankle, knee, and hip recalls. Despite this, the FDA advises against using these potentially defective shoulder systems. 
  • March 2024: Exactech recalled its Equinoxe Shoulder System devices to clear up market confusion and concerns.

Exactech Recall Updates in 2024

Here’s the latest on the Exactech knee and hip replacement recall as of 2024:

  • Hip Replacement Recall 2024: Exactech took action in January 2024 by issuing an Urgent Medical Device Recall for the AccuMatch Hip System, extending it to include all hip devices with polyethylene components packed in faulty bags. This recall affects around 657,391 devices, including hip, knee, ankle, and shoulder replacements manufactured between 2004 and August 2021. 
  • Knee Replacement Recall 2024: The Exactech knee replacement recall has seen expansions to include additional models, leading to a surge in lawsuits from affected patients. The FDA has been closely monitoring developments, issuing alerts to healthcare providers and patients.

Impact of the Recall

The recall of Exactech’s joint replacement devices has had significant effects on patients, healthcare providers, and the medical device industry. It has raised awareness about the risks of certain implants and emphasized the need for strict quality control in manufacturing and packaging.

  • The Healthcare providers: Healthcare providers face the challenge of identifying and supporting patients with affected implants. They may need to perform additional screenings, tests, or follow-up appointments to check for device failure or complications. 
  • The Medical device industry: The recall also impacts the medical device industry, highlighting the necessity for stronger oversight and regulation to ensure implant safety. Regulatory agencies might enforce stricter guidelines for manufacturers to prevent similar issues in the future. 
  • The Patients: For patients, the recall has created concerns about the safety and reliability of their implants. Many are anxious or uncertain about the integrity of their devices and may need extra monitoring or medical care.

Health Risks and Complications

Patients with Exactech joint replacement devices should watch for signs of potential issues. Common symptoms include:

  • Bone fracture: Stress fractures or bone damage near the joint. 
  • Bone loss: Reduced bone density around the implant, weakening the joint. 
  • Device malfunction: Sudden changes like locking, seizing, or malfunctioning. 
  • Excessive wear: Premature wear of implant components, risking failure. 
  • Grinding or clicking: Sensations of grinding, clicking, or popping in the joint. 
  • Implant fracture: Breakage of implant materials causing instability. 
  • Increased pain: Persistent or worsening joint pain without a clear cause. 
  • Instability or weakness: Feeling of instability or weakness, especially during weight-bearing. 
  • Limited mobility: Difficulty moving the joint or reduced range of motion. 
  • Need for revision surgery: Additional surgery may be required to fix implant-related issues, posing risks like infection, nerve damage, and extended recovery. 
  • Pain: Chronic or severe joint pain, tenderness, or sensitivity. 
  • Premature failure: Early failure of the implant, requiring revision surgery. 
  • Swelling or inflammation: Swelling, redness, or inflammation around the joint.

Patients should promptly report any concerning symptoms to their healthcare provider for a thorough evaluation. Early detection and intervention are crucial for addressing defective Exactech devices and minimizing complications.

New Treatments for Those Affected by the Exactech Recall

For those experiencing hip replacement recall symptoms or knee replacement recall symptoms, treatment options include:

  • Pain management: Medications and injections to alleviate discomfort and inflammation. 
  • Physical therapy: Tailored exercises to strengthen muscles and improve mobility. 
  • Revision surgery: In severe cases, replacing the defective implant with a more reliable one may be necessary.

Consulting healthcare professionals is vital to determine the best treatment based on individual symptoms and medical history, ensuring effective management and improved quality of life.

FDA Recommendations

For Patients

  • No symptoms: If your Exactech knee, ankle, or hip replacement device is working well and you have no pain or symptoms, the FDA does not recommend surgery to remove it. 
  • New symptoms: Contact your healthcare provider if you experience new or worsening pain, swelling, inability to bear weight, grinding noises, or weakness around your implant. 
  • Check recall: If you have a knee or ankle replacement, use Exactech’s online database to see if your implant is part of the recall. You will need your device serial number.

For Healthcare Providers

  • Do not implant recalled devices: Avoid using any recalled Exactech knee, ankle, or hip devices. 
  • No removal if asymptomatic: Do not remove well-functioning Exactech devices from patients who do not have new or worsening pain or symptoms. 
  • Monitor patients: Keep an eye on patients with Exactech implants manufactured between 2004 and August 2021 for potential wear, failure, or bone loss. Consider X-rays if you suspect device failure. 
  • Discuss revision surgery: Talk about revision surgery with patients experiencing worsening pain or joint weakness potentially due to the implant. Discuss the benefits and risks of all treatment options. 
  • Remove recalled devices: Remove all recalled devices from inventory and return them to Exactech. 
  • Visit recall website: For more information about the recalled devices, visit the Exactech Recall website.

Reporting a Defective Exactech Device to the FDA

If you have a defective Exactech device and want to report it to the FDA, follow these steps:

  • Visit the FDA’s MedWatch website. Go to the FDA’s MedWatch Reporting System online. 
  • Select “Report a Problem.” Choose the option to report a problem with a medical device. 
  • Fill out the form:

  • Personal information: Provide your contact details. 
  • Device information: Include details about the Exactech device, such as the model, serial number, and date of implantation. 
  • Description of the issue: Describe the problem you experienced with the device. Include information about any symptoms, pain, or complications you faced. 
  • Health professional information: If applicable, provide information about the healthcare professional who treated you.
  • Submit the report: Once you have completed the form, submit it through the online system. 
  • Follow-up: After submitting the report, you may receive a confirmation email from the FDA. Keep this for your records. The FDA may contact you for additional information if needed.

Alternative methods to report:

  • By fax: Fax the completed MedWatch Form FDA 3500 to 1-800-FDA-0178. 
  • By mail: Download the MedWatch Form FDA 3500, fill it out, and mail it to:

MedWatch 

5600 Fishers Lane 

Rockville, MD 20852-9787

  • By phone: Call the FDA’s MedWatch Hotline at 1-800-FDA-1088 to report the defective device.

Reporting the defective device helps the FDA monitor the safety and effectiveness of medical devices and take necessary actions to protect public health.

How to Check If You Have a Recalled Exactech Implant

In these steps, patients can determine if they have a recalled Exactech implant and take appropriate action to address any potential issues:

  • Check the Exactech website: Visit the Exactech website and use the serial number of your implant to check if it is affected by the recall.

Exactech Recall Information 

Exactech Serial Number Lookup 

 

  • Check the FDA website: Visit the FDA website and search for medical device recalls. Enter the device name, model number, or serial number to check if it is listed under a recall. 
  • Check your medical records: Review your medical records to find the serial number of your implant. This information can help determine if your implant is recalled. 
  • Contact Exactech directly: Call Exactech at 1-888-912-0403 to inquire about the status of your implant. 
  • Contact your surgeon: Inquire with your surgeon or healthcare provider about the status of your implant. They may already have information about the recall and can guide you on the next steps. 
  • Monitor for symptoms: Be vigilant for symptoms like pain, swelling, or instability in your implant. If you experience any of these symptoms, contact your surgeon or healthcare provider for further evaluation.
 

What to Do if You Are Having Problems with Your Knee or Hip Implants

If you’re experiencing issues with your knee or hip implants, consult your orthopedic surgeon or a medical professional. Follow these steps to ensure proper care:

  • Report your symptoms: Inform your surgeon about any pain, swelling, or discomfort in your knee or hip. Be specific about the location, duration, and severity. 
  • Schedule a follow-up appointment: Set up a follow-up appointment to discuss your symptoms and concerns. This helps your surgeon assess the situation and determine the best course of action. 
  • Imaging tests: Your surgeon may recommend imaging tests like X-rays, MRI, or CT scans to examine the implants and surrounding tissues. These tests can identify potential issues or complications. 
  • Treatment options: Based on the diagnosis, your surgeon may suggest pain management, physical therapy, or surgical intervention. 
  • Revision surgery: If necessary, your surgeon may recommend revision surgery to replace the damaged implants with new ones. 
  • Antibiotic treatment: If an infection is suspected, your surgeon may prescribe antibiotics. This might involve intravenous antibiotics and follow-up blood work to monitor effectiveness. 
  • Follow-up care: After treatment, follow up with your surgeon to ensure the issue is resolved and address any ongoing concerns. Monitor for signs of infection, such as fever, swelling, or redness. 
  • Consider a second opinion: If you’re not satisfied with the treatment or diagnosis, seek a second opinion from another orthopedic surgeon or joint replacement specialist. 
  • Consult with a lawyer: If you’ve experienced complications due to a defective Exactech implant, consider consulting a product liability lawyer to seek compensation for your damages.

Legal Options for Those Affected by the Exactech Recall

If you or a loved one has been impacted by the Exactech recall, it’s important to know these legal options:

  • Consult a legal expert: If you’ve been harmed by a defective Exactech implant, consult a lawyer specializing in product liability and medical device litigation. They can evaluate your case and guide you on your options. 
  • Class action lawsuits: Many people harmed by the same defective product can join a class action lawsuit against the manufacturer, pooling resources for collective compensation. 
  • Multidistrict litigation (MDL): Similar claims against the same defendant can be consolidated into MDL for efficient pretrial proceedings. As of May 2024, 1,462 lawsuits against Exactech were in MDL 3044 in the U.S. District Court for the Eastern District of New York. 
  • Product liability lawsuits: If you’ve been injured by a defective Exactech implant, you may file a product liability lawsuit, proving the defect and its direct impact on your health. 
  • Settlement negotiations: Manufacturers might settle claims out of court to avoid prolonged litigation. Settlements provide financial compensation without a trial. 
  • Ankle, hip, shoulder, or knee replacement lawsuit statute of limitations: Act quickly as there are time limits for filing Exactech lawsuits. Consult an attorney promptly to ensure your claim is filed on time.

If affected by the Exactech recall, seek legal guidance to protect your rights and pursue compensation.

Why File an Exactech Lawsuit?

If you’ve experienced harm or complications from defective implants, filing an Exactech lawsuit can be crucial. Here’s why:

  • Holding Exactech accountable: By taking legal action, you’re not just seeking compensation. You’re also holding the manufacturer accountable for their products’ safety and quality. This sends a message that negligence won’t be tolerated. 
  • Preventing further harm: Your Exactech recall lawsuit can help raise awareness of the risks associated with these implants. This can prompt regulatory agencies to tighten oversight and implement stricter safety measures, protecting future patients. 
  • Seeking compensation: It’s about more than just covering medical bills. Compensation can also address lost wages, ongoing treatment costs, and the pain and suffering endured. 
  • Seeking justice: Filing an Exactech lawsuit is often about seeking justice for the harm you’ve endured. It provides an opportunity for your voice to be heard and for accountability to be upheld. 
  • Spurring product improvements: Lawsuits involving defective medical devices can drive improvements in product design, manufacturing processes, and safety standards. Your legal action could help prevent similar issues from occurring in the future, benefiting countless others.

Filing an Exactech recall lawsuit is a significant decision that should be carefully considered. Consulting with an experienced attorney specializing in product liability and medical device litigation can provide valuable guidance and support throughout the legal process.

Criteria for Joining the Exactech Lawsuit

To participate in an Exactech recall lawsuit, individuals generally must meet the following criteria:

Exactech product:

  • Opterack Logic   
  • Optetrack   
  • Received a knee, hip or ankle joint but unsure of manufacturer  
  • Truliant   
  • Vantage   

 

  • Replacement date: After 2004 
  • Replacement procedure: Knee, hip, and ankle replacement 
  • Target Location: Nationwide

Process for Filing an Exactech Recall Lawsuit

If you or a loved one have been affected by a defective Exactech implant, consider legal action for compensation. Here’s a brief guide:

  • Consult with a personal injury attorney: Start by consulting an experienced attorney in medical device litigation. They will evaluate your case, discuss options, and explain the process. 
  • Gather medical records and evidence: Collect medical records, surgery details, and documentation of complications. This helps your attorney build a strong case. 
  • File the complaint: Your attorney will draft and file a complaint against Exactech, outlining your injuries and the damages sought. 
  • Discovery phase: Both parties exchange information, request documents, take depositions, and gather testimony from experts. 
  • Negotiation and settlement: Attempt to negotiate a fair settlement. If unsuccessful, prepare for trial. 
  • Trial: Your attorney presents your case to a judge or jury, using evidence and expert testimony to prove the defective implant caused your injuries. 
  • Post-trial actions: If you win, the court will determine your compensation. Your attorney guides you through any post-trial motions or appeals.

Filing an Exactech lawsuit can be complex, but it’s crucial for seeking justice and preventing future incidents with defective medical devices.

 

Causes of Action in Exactech Recall Lawsuit

When suing Exactech for defective implants, your legal claim will be based on specific causes of action. These form the foundation of your case. Here are common causes of action in an Exactech recall lawsuit:

  • Breach of warranty: Exactech breached warranties of fitness, merchantability, and implied warranties, leading to implant failure. 
  • Design defect: The implants were designed with defects that made them unreasonably dangerous and prone to failure. 
  • Failure to recall: Exactech did not recall the defective implants in a timely manner, causing further injuries and damages. 
  • Failure to warn: Exactech did not provide adequate warnings to doctors and patients about the risks, resulting in injuries. 
  • Manufacturing defect: The implants were manufactured with defects making them dangerous and likely to fail. 
  • Marketing defect: Exactech misrepresented the safety and effectiveness of the implants, leading to injuries. 
  • Negligence: Exactech failed to exercise reasonable care in designing, manufacturing, and testing the implants, causing premature failure. 
  • Product liability: The implants were defective and dangerous, and Exactech knew or should have known about these defects. 
  • Punitive damages: Seeking punitive damages for Exactech’s reckless disregard for patient safety. 
  • Strict liability: The implants were defective and dangerous at the time of sale, and Exactech should have known about the defects.

Key Evidence for a Strong Exactech Lawsuit

To build a compelling Exactech recall lawsuit, gathering comprehensive evidence is crucial. Here are the key pieces of evidence that can significantly strengthen your case:

  • Device information: Details about the specific implant, including the serial number, model, and manufacturer documentation. 
  • Doctor’s reports: Detailed notes from treating physicians outlining the patient’s condition, treatments, and any complications resulting from the defective device. 
  • Expert testimony: Statements from medical experts who can attest to the device’s defects and the harm it caused to the patient. 
  • Financial documentation: Records showing medical expenses, lost wages, and other financial impacts caused by the defective implant. 
  • Injury documentation: Evidence of the injuries and complications experienced, such as pain, swelling, bone loss, or implant failure. 
  • Medical records: Comprehensive medical records documenting the original implantation, any complications, and subsequent surgeries related to the recalled Exactech device. 
  • Product data: Information on the design, manufacturing, and testing of the device to help establish manufacturer liability. 
  • Revision surgery records: Documentation of any surgeries performed to correct issues caused by the recalled device. 
  • Visual evidence: Photos and videos documenting the device, the patient’s condition, and any relevant medical procedures. 
  • Witness statements: Testimonies from witnesses who can confirm the patient’s condition and the impact of the defective device.

Collecting this evidence is vital to building a strong case against Exactech and securing the compensation you deserve for the harm caused by their defective implants.

Statute of Limitations

The deadline for filing an Exactech knee replacement lawsuit varies by state. Act promptly and seek legal advice to ensure you don’t miss this deadline. Your attorney can help you understand the specific timeframe in your state and assist with filing your claim on time.

Potential Damages in Exactech Lawsuits

In Exactech knee replacement lawsuits, individuals seek various forms of compensation to address damages caused by defective implants. This includes:

  • Disability and impairment: Compensation for permanent disabilities affecting daily life, work, or enjoyment. 
  • Legal fees and costs: Reimbursement for expenses in pursuing the lawsuit, like attorney’s fees and court costs. 
  • Loss of consortium: Compensation for strain on relationships due to injuries and disabilities. 
  • Lost income: Compensation for past and future income lost from work disruptions caused by the defective implants. 
  • Medical expenses: Reimbursement for all medical costs, including surgeries, medications, and rehabilitation. 
  • Pain and suffering: Monetary compensation for physical and emotional suffering due to the implants. 
  • Punitive damages: Awarded for extreme negligence, aiming to punish the company and deter future misconduct. 
  • Rehabilitation and therapy: Coverage for ongoing treatment to improve physical and emotional well-being.

These aim to address hardships caused by defective Exactech implants, aiding in recovery and moving forward.

Exactech Lawsuit Payout

The Exactech lawsuit payout amounts vary based on factors like injury severity and medical expenses. Here are estimated settlement amounts:

  • Exactech ankle implant lawsuits. $125,000 to $250,000. 
  • Exactech hip replacement lawsuits. $250,000 to $300,000. 
  • Exactech knee implant lawsuits. $100,000 to $225,000.

These figures are based on average payouts in similar cases. Actual amounts may differ depending on individual circumstances. An experienced attorney can help determine appropriate compensation and represent you in court.

The Importance of a Personal Injury Lawyer

Dealing with the aftermath of a defective medical device like the recalled Exactech implants can be daunting. That’s where a skilled personal injury lawyer comes in. Here’s why having one is crucial:

  • Building a strong case: A lawyer gathers and analyzes evidence, like medical records, to build a solid case for you. 
  • Contingency fee arrangement: Most personal injury lawyers work on a “no win, no fee” basis, making legal representation affordable. 
  • Specialization in medical device cases: These lawyers know the ins and outs of defective medical device cases, ensuring effective handling. 
  • Holding Exactech accountable: Legal action holds Exactech responsible for their faulty products, preventing similar issues in the future. 
  • Maximizing compensation: Experienced lawyers accurately assess your claim’s value, ensuring you get the maximum compensation. 
  • Navigating legal procedures: They guide you through the legal process, ensuring paperwork is correct and deadlines are met. 
  • Negotiating with insurance companies: Lawyers negotiate with insurers to ensure you get a fair settlement, not a minimized payout. 
  • Providing peace of mind: Handling legal matters lets you focus on recovery, reducing stress during a tough time. 
  • Representing you in court: If needed, they’ll represent you in court, presenting your case effectively and arguing on your behalf. 
  • Understanding settlement options: Lawyers help you grasp settlement options, advising on whether to accept or pursue further action.

Hire Ethen Ostroff Law

Looking for legal assistance with your Exactech case? Consider hiring Ethen Ostroff Law. Our team is dedicated to supporting you throughout the legal process, from consultation to resolution. We understand the challenges you’re facing. Trust us to provide personalized support and professional legal guidance as we work to secure the compensation you deserve. Contact us today to learn more about how we can assist you.

Frequently Asked Questions About Exactech Lawsuits

Settlement amounts in Exactech lawsuits can vary based on individual circumstances, including the severity of the injuries and associated costs. Estimates suggest potential Exactech knee replacement lawsuit settlement amounts range from $100,000 to $300,000 per plaintiff, though actual compensation will vary based on the severity of the damage.

To qualify for an Exactech lawsuit, you typically need to have received a defective Exactech knee or hip implant and experienced complications or symptoms related to the defect. Medical documentation of the implant and related issues is also required.

Settlements can range widely.  The value of a knee replacement lawsuit depends on several factors, including the extent of your injuries, medical expenses, lost wages, and pain and suffering. An attorney can provide a more accurate estimate based on your case.

The TPG Exactech lawsuit involves legal action against TPG Capital, which acquired a majority stake in Exactech. These lawsuits claim that TPG Capital and Exactech are responsible for the defective implants and the injuries caused to patients.

Exactech lawsuit settlement timelines vary. Cases may settle in months or years, depending on complexity and plaintiffs. Your attorney can give a more precise estimate based on your case.

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While in law school, he distinguished himself as Executive Editor of JURIS Magazine, received the prestigious CALI Excellence for the Future Award, and completed five hands-on internships that laid a strong foundation for his legal career.


Nicholas began his post-graduate career clerking for the Honorable Linda Rovder Fleming in the Cambria County Court of Common Pleas. From there, he quickly found his calling in workers’ compensation, personal injury, and Social Security disability law—areas where he could directly impact people’s lives in moments of crisis. He’s helped clients navigate complex legal claims, including securing a settlement exceeding $300,000.

Nicholas brings clear communication, genuine empathy, and an unrelenting drive to achieve the best outcomes for his clients. Whether he’s navigating a complex workers’ comp claim or pushing for a major settlement, he brings focus, dedication, and deep legal knowledge to every case.

He’s also a proud member of Pennsylvania Advocates for Justice and remains active in various professional legal organizations. Nicholas is licensed to practice law in Pennsylvania.

When he’s not fighting for the injured, Nicholas is enjoying time with his family, kicking a soccer ball around, hitting the golf course, or cheering on Pittsburgh’s local teams.

Joe Ring heads the workers’ compensation department at Ethen Ostroff Law, where he takes pride in fighting for injured workers.

Joe is a Philadelphia native and maintains deep roots in the area.  As the grandson of a Philadelphia Firefighter, son of a Philadelphia public school teacher, and veteran of the United State Marine Corps, he was taught to value service, dedication, and hard work.   He applies these values to every case and takes great satisfaction in representing hard-working clients with those same traits.

After obtaining his bachelor’s degree in history from St. Vincent College in Western Pennsylvania, he graduated from Villanova Law School in 2012 and, since then, has litigated hundreds of workers’ compensation hearings and trial depositions on behalf of both employers and injured workers.  During this time, Mr. Ring has written articles and presented Continuing Legal Education courses on developments in Pennsylvania Workers’ Compensation Law.  He is active in local professional organizations, and, in 2022, he served a Co-chairperson of the Philadelphia Bar Associations Workers’ Compensation Section.

Since coming to EOL in 2024, he has dedicated his practice entirely to helping injured workers navigate the system and obtain their rightful benefits.

Joe is licensed to practice in Pennsylvania.

Brandon Zanan heads the personal injury claim department with Ethen Ostroff Law.

Brandon’s education in both law and medicine assist him in expertly representing badly injured victims. Brandon has a Master’s Degree in Forensic Medicine from the Philadelphia College of Osteopathic Medicine, with a concentration in anatomy and pathology. With this knowledge,  Brandon is skilled at analyzing medical records and understanding injuries that are common in personal injury claims. He uses this expertise in conjunction with listening carefully to each client’s needs, in order to fiercely advocate for clients and tell their stories when they would not otherwise have a voice.

Brandon’s background includes a variety of experience and skills in various areas of civil practice. He is the author and editor of numerous books for the George T. Bisel Publishing Company, including “Pennsylvania Damages” and the “Pennsylvania Vehicle Code Annotated,” two texts that are frequently relied on by lawyers and judges across Pennsylvania as authoritative resources on personal injury law.

Brandon is a member of the Pennsylvania and Montgomery Bar Associations. He is also a member of Pennsylvania Association for Justice, and has served as an executive board member of the Montgomery American Inn of Court.

He is admitted to practice in the Commonwealth of Pennsylvania, the United States District Courts for the Eastern District of Pennsylvania and Middle District of Pennsylvania, the State of New Jersey, the United States District Court for the District of New Jersey, and in the Commonwealth of Virginia. Brandon has represented many clients in motor vehicle, premises liability, animal bite, and products liability cases across Pennsylvania and New Jersey and has obtained outstanding results with millions of dollars recovered for his clients.

He has been named a Pennsylvania Rising Star from 2021 onward. The “Super Lawyers-Rising Star®”, list recognizes no more than 2.5 percent of attorneys in each state

Brandon currently lives in Malvern with his wife Rachel and their son Max.

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When you opt-in, you will receive text messages (SMS/MMS) on your mobile number. These messages may contain information about your case, and the message frequency may vary from user to user. Please note that message and data rates may apply. If you wish to opt out of this service, you can do so anytime by simply texting “STOP” to the phone number. Once you text “STOP” to us, we will send you an SMS to confirm that you have been unsubscribed. If you encounter any issues, you can reply with the keyword “HELP” to get assistance. Please be aware that carriers are not responsible for any delayed or undelivered messages.

By providing your phone number and submitting a form on our website, you consent to receive communications, including automated calls, texts, and pre-recorded messages, from EO and its affiliates. These communications may include updates about your case, promotional offers, and other information. You understand that these calls may be generated using automated technology, and that standard message and data rates may apply.

Your consent to receive automated calls is not a condition of any purchase or service. By checking the consent box on our contact form or by calling our firm, you agree to these Terms and Conditions and provide your written consent to receive these communications. You may opt out of these communications at any time by replying STOP to any text message or by contacting us at [insert contact information].

State-Specific Compliance

EO complies with all federal and state laws regarding automated calls and telemarketing practices. Certain states have additional restrictions on the use of automated dialing systems and pre-recorded messages. The following states have more restrictive regulations:

  • California: Requires prior express written consent for automated calls.
  • Florida: Requires prior express written consent for automated calls and texts.
  • New York: Requires prior express written consent for automated calls.
  • Texas: Requires prior express written consent for automated calls.

If you are a resident of one of these states, EO will obtain your prior express written consent before making any automated calls or sending pre-recorded messages to you.

By submitting a form inquiry or calling our firm, you agree to us contacting you, and your checking the box when submitting your form inquiry serves as written consent.

Information and Legal Disclaimer

The information contained in this website is for informational purposes only, and should not be construed as legal advice. Testimonials and case results contained in this website are for demonstrative purposes only, and do not constitute a guarantee of any particular outcome in a specific case.

By requesting a free consultation with Ethen Ostroff Law, PLLC, you agree to the following:

  • Any information I submit is for review only, and there will be no charge for the initial consultation.
  • I have not entered into an attorney-client relationship with Ethen Ostroff Law, PLLC until such time as a formal written Retainer Agreement is signed by myself and a representative of Ethen Ostroff Law, PLLC. There is no guarantee that Ethen Ostroff Law, PLLC will accept my case.
  • Any information received by Ethen Ostroff Law, PLLC, prior to the execution of a written Retainer Agreement, is not subject to the Attorney-Client Privilege and is not considered confidential.
  • Additional information may be requested in order for Ethen Ostroff Law, PLLC to make a decision on whether or not to accept my case.
  • Because no attorney-client relationship has been established, I will remain personally responsible to meet all necessary deadlines applicable to my claim, until such time as Ethen Ostroff Law, PLLC makes a final decision. I acknowledge that I have not received any representations or legal opinions with respect to any time frames or deadlines that may be applicable to my claim.

No Relationship or Obligation Arises from Use of the Site

The law differs in every jurisdiction, and you should not rely on any opinion except that of an attorney you have retained, who has a professional duty to advise you after being fully informed of all the pertinent facts, and who is licensed in the applicable state, and is familiar with the applicable law. Internet subscribers, mobile application users, and online readers should seek professional counsel about their legal rights and remedies. You should not act or refrain from acting on the basis of any information found on the Site. Any actions or decisions about your legal rights should be based on the particular facts and circumstances of your situation, and appropriate legal advice from an attorney retained directly by you. EO EXPRESSLY DISCLAIMS ALL LIABILITY WITH RESPECT TO ACTIONS TAKEN OR NOT TAKEN BASED UPON ANY INFORMATION OR OTHER CONTENTS OF THIS SITE. Viewing the Site, or communicating with EO by Internet e-mail or through the Site does not constitute or create an attorney-client relationship with anyone. The content and features on the Site do not create, and are not intended to create, an attorney-client relationship, and shall not be construed as legal advice. The content and features of the Site, including means to submit a question or information, do not constitute an offer to represent you or otherwise give rise to an attorney/client relationship.

THE SITE IS PROVIDED “AS IS”. EO MAKES NO WARRANTIES, EXPRESS OR IMPLIED, REGARDING THE SITE AND ONLINE SERVICES AND HEREBY DISCLAIMS ALL WARRANTIES OF ANY KIND OR NATURE, INCLUDING, WITHOUT LIMITATION, THE IMPLIED WARRANTIES OF MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE, ACCURACY, AND NON-INFRINGEMENT. WITHOUT LIMITING THE FOREGOING, EO DOES NOT GUARANTEE THAT THE ONLINE SERVICES OR PRODUCTS WILL MEET YOUR REQUIREMENTS, OR WILL BE ERROR-FREE, UNINTERRUPTED, OR FREE OF VIRUSES OR OTHER HARMFUL COMPONENTS, OR THAT ANY DEFECTS WILL BE CORRECTED.

Accounts

To use some features of the Site, you may be required to create an account. In connection therewith, you agree to provide and maintain true, accurate, current, and complete information about yourself. You are responsible for maintaining the confidentiality of the information you hold for your account login, including your password, and for all Submissions made from your account. You agree to notify us immediately of any unauthorized use of your login. EO may suspend access to your account if it suspects illegal or improper use, or for other reasons, such as for account management purposes, at its sole discretion.

Confidentiality is Not Guaranteed

Information sent to Ethen Ostroff Law, PLLC. via Internet e-mail or through the Site is not secure and is done on a non-confidential basis. EO may make reasonable efforts to keep communications private, but because of the nature of Internet communications and the absence of an attorney/client relationship, we cannot promise or guarantee confidentiality.

DISCLAIMER – This Site Does Not Provide Medical Diagnosis or Advice

The content provided on the Site, such as documents, text, graphics, images, videos, news alerts, pharmaceutical drug recalls, prescription medication history, or information on litigation concerning the foregoing topics, or other materials, is for informational purposes only. The information is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always consult a physician for diagnosis and treatment of any medical condition or for any questions you may have regarding a health concern. Never disregard professional medical advice, alter a prescription plan in any way, or delay or refrain from seeking medical advice because of something you have read or seen on the Site. Links to other sites are provided for information only. Use of trade names is for identification only and does not constitute endorsement by EO.

Without limiting the generality of the foregoing, the Site may present information about pharmaceutical drug recalls, which is for information purposes only. Such information is not necessarily the most current information on the subject and may or may not be updated based on the last information concerning such recalls. Do not make any decisions regarding medication or medical providers based on information from the Site, including but not limited to information we provide about drug recalls.

EO Is Not Responsible for Content; Limitation on Liability

EO may periodically change, remove, or add the material on the Site without notice. This material may contain technical or typographical errors. EO DOES NOT GUARANTEE ITS ACCURACY, COMPLETENESS OR SUITABILITY. EO assumes no liability or responsibility for any errors or omissions in the contents of the Site. Your use of the Site is at your own risk. Under no circumstances shall EO or any other party involved in the creation, production, or delivery of the Site be liable to you or any other person for any indirect, special, incidental, or consequential damages of any kind arising from your access to, or use of, the Site. TO THE MAXIMUM EXTENT PERMITTED BY APPLICABLE LAW IN NO EVENT SHALL EO BE LIABLE FOR ANY SPECIAL, INDIRECT, OR CONSEQUENTIAL DAMAGES RELATING TO THIS MATERIAL, FOR ANY USE OF THIS WEBSITE, OR FOR ANY OTHER LINKED WEBSITE.

Third-party Web Sites

The Site contains links to third-party websites for the convenience of our users. EO does not endorse any of these third-party sites and does not imply any association between EO and those sites. EO does not control these third-party websites and cannot represent that their policies and practices will be consistent with these Terms of Use. If you use links to access and use such websites, you do so at your own risk. EO is not responsible for the contents or availability of any linked sites. These links are provided only as a convenience to the recipient. These Terms only apply to the Site and do not apply to any linked sites. We encourage you to read and understand the terms of use of any linked sites that you visit. Links do not imply that we sponsor, endorse, are affiliated with or associated with, or are legally authorized to use any trademark, trade name, service mark, design, logo, symbol, or other copyrighted materials displayed on or accessible through any linked site.

EO Clients

Only individuals who have entered into a mutually signed retainer agreement with EO are EO clients (“EO Clients”).

Legal and Ethical Requirements

EO has tried to comply with all legal and ethical requirements in compiling the Site. We welcome comments about our compliance with the applicable rules and will update the Site as warranted, upon learning of any new or different requirements.

Ethen Ostroff Law reserves the right to refer or sell leads that come through any of Ethen Ostroff Law’s marketing.

Ethen Ostroff Law also may sell leads on certain campaigns generated in association with third party marketing companies.

Governing Laws in Case of Dispute; Jurisdiction

These Terms of Use shall be governed by and construed in accordance with the laws of the State of Pennsylvania, USA, without regard to any choice of law principles. Any and all disputes arising hereunder shall be governed as set forth in the Arbitration section below.

Submissions

You are solely responsible for any information, content, or material you transmit to or through the Site (“Submissions”). You understand that Submissions are considered non-confidential and non-proprietary. Furthermore, you grant EO an unrestricted, irrevocable, perpetual, transferable, sublicensable, worldwide, royalty-free license to use, copy, reproduce, display, publish, publicly perform, transmit, and distribute any Submission, without compensation or accounting to you or anyone else. You represent and warrant that: (a) you have the right to submit the Submission to EO and grant the licenses as described above; (b) EO will not need to obtain licenses from any third party or pay royalties to any third party for its use of the Submission; (c) the Submission does not infringe any third party’s rights, including intellectual property rights and privacy rights; and (d) the Submission complies with these Terms of Use and all applicable laws and regulations.

EO takes no responsibility and assumes no liability for any Submission.

Arbitration

Any and all claims by you arising out of or related to the Site or your use thereof may be resolved only through a binding arbitration proceeding to be conducted under the auspices of the Commercial Arbitration Rules of the American Arbitration Association in Montgomery County, Pennsylvania. Both your agreement to arbitrate all controversies, disputes and claims, and the results and awards rendered through the arbitration, will be final and binding on you and may be specifically enforced by legal proceedings. Arbitration will be the sole means of resolving such controversies, disputes and claims, and you waive your rights to resolve such controversies, disputes and claims by court proceedings or any other means. You agree that judgment may be entered on the award in any court of competent jurisdiction and, therefore, any award rendered shall be binding. The arbitrator may not consolidate more than one person’s claims, and may not otherwise preside over any form of a representative or class proceeding. You understand that by agreeing to arbitration as a mechanism to resolve all controversies, disputes and claims between us, you are waiving certain rights, including the right to bring an action in court, the right to a jury trial, the right to broad discovery, and the right to an appeal. You understand that in the context of arbitration, a case is decided by an arbitrator (one or more), not by a judge or a jury.

International Use

The Site is controlled, operated, and administered by EO from offices within the United States of America and is only intended for use therein. We make no representation regarding use of the Site outside of the United States.

Other Terms

If, for any reason, our Terms of Use, Privacy Policy, or any portion thereof to be unenforceable, such provision shall be enforced to the maximum extent permissible so as to give the intended effect thereof, and the remainder of these Terms of Use and Privacy Policy shall continue in full force and effect. EO’s failure to act with respect to a breach by you or others does not waive our right to act with respect to that breach or subsequent or similar breaches. No consent or waiver by EO hereof will be deemed effective unless in writing. These Terms of Use, together with our Privacy Policy, as each is currently posted, constitute the entire agreement between EO and you with respect to your use of the Site and supersede all previous written or oral agreements relating to the subject matter hereof, that this agreement shall not supersede, restrict, or replace any agreements governing the attorney-client relationship between EO and EO Clients.

EO may, in its sole discretion and without prior notice, block and/or terminate your access to the Site and if we determine that you have violated these Terms of Use or other terms or agreements or that may be associated therewith or if you use the Site in a way that we deem, in our sole discretion, to be an unacceptable use.

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Disclaimer: By submitting the form above and checking the consent box, you agree to our conditions and privacy policy and permit Ethen Ostroff Law to contact you via text messages, phone calls. Standard message rates may apply.