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Exactech Lawsuit: Seeking Compensation for Premature Wear of Implants

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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.


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.

His career began in public service as a Surveillance Officer in Maricopa County, where he gained firsthand experience in high-stakes decision-making and developed a deep sense of discipline and accountability. He later served as Chief Operating Officer of a fast-growing law firm, driving efficiency, revenue growth, and team development. Today, Ryan focuses on helping law firms reach their full potential by aligning people, processes, and long-term vision. A strategic thinker and empowering leader, Ryan is passionate about developing others and guiding organizations through meaningful, lasting growth.

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These tools may collect the information listed in section 3. If you give us your email address or phone number, a scrambled (hashed) version may be sent to an advertising platform so it can match your visit to an existing account.

Google, Meta, TikTok, and Reddit may combine the information they receive with other data they hold about you and use it under their own privacy policies. You can learn how Google uses information from sites that use its services at  policies.google.com/technologies/partner-sites.

9. Your choices

  • Block or delete cookies in your browser settings. Some parts of the Site may not work as expected if you do.
  • Change your ad settings directly in your Google, Meta, TikTok, or Reddit account.
  • Manage Google ad personalization at  myadcenter.google.com.
  • Install the Google Analytics opt-out browser add-on at  tools.google.com/dlpage/gaoptout.
  • Opt out of interest-based ads from participating companies at  optout.aboutads.info.
  • Reply STOP to any text message to stop receiving texts.
  • Contact us using the information in section 15 to ask us to stop using your information for advertising.

10. Residents of certain states

Some state privacy laws, including California’s, may treat sharing information through advertising pixels as a “sale” or “sharing” of personal information, or as targeted advertising. Depending on where you live, you may have the right to know what information we hold about you, to ask us to correct or delete it, and to opt out of its sale or sharing. To make a request, contact us using the information in section 15. We may need to verify your identity before we respond. We will not treat you differently for using these rights.

11. How we protect your information

We use reasonable administrative, technical, and physical safeguards to protect your information. No method of sending or storing data over the internet is completely secure, so we cannot guarantee the security of information you send us.

12. How long we keep your information

We keep your information as long as we need it for the purposes described in this policy, including to meet legal, ethical, and record-keeping obligations.

13. Children’s privacy

The Site is not directed to children under 13, and we do not knowingly collect personal information from them online. If a parent or guardian is contacting us about a child’s injury, the parent or guardian should submit the inquiry.

14. Changes to this policy

We may update this policy when we add, change, or remove tools on the Site or change how we handle information. We will post the updated version here and change the effective date above.

15. Contact us

If you have questions about this policy or want to make a privacy request, contact us:

  • Phone: 610-510-8883
  • Email: intake@ethenostrofflaw.com
  • Mail: Ethen Ostroff Law, PLLC, 21 E 5th Ave, Suite 102, Conshohocken, PA 19428

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