BioZorb

BioZorb was designed to help breast cancer patients heal after surgery. Marketed as a surgical marker that supports tissue regrowth and guides radiation treatment, it was implanted in thousands of women across the country. But for many, this once-promising device became a source of pain, inflammation, and permanent damage.

If you or a loved one suffered complications after receiving a BioZorb implant, you may be eligible to file a lawsuit. A BioZorb Lawsuit Lawyer can help you understand your rights and pursue compensation. Patients have reported severe reactions to the device, including chronic pain, hard tissue buildup, infections, and the need for additional surgery to remove it.

At Ferrer Poirot Feller, we help people nationwide hold medical device manufacturers accountable for products that cause more harm than healing. BioZorb was supposed to support recovery, not destroy quality of life. If it failed you, we’re here to help you take the next step.

You don’t have to go through this alone, and you don’t pay anything unless we win.

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Why Hire a BioZorb Lawsuit Lawyer?

BioZorb complications aren’t just frustrating—they’re traumatic. Many women assumed the implant was safe and necessary, only to discover later that it caused pain, disfigurement, or had to be surgically removed. Worse, most patients say they were never properly warned about the risks.

Hiring a BioZorb Lawsuit Lawyer gives you the power to hold the manufacturer accountable.

At Ferrer Poirot Feller, we understand what you’ve been through. We’ve helped clients across the country pursue justice after defective medical devices disrupted their lives. Call a Lawyer who can investigate your surgical records, document the complications, and work with medical experts who can explain exactly what went wrong.

Whether you had unexpected pain, inflammation, infection, or needed revision surgery, we’re here to build your case from the ground up and fight for full compensation.

If you’re living with the aftermath of a BioZorb implant, let us help you understand your legal options and pursue justice.

You’re Not the Only One—Women Across the Country Are Speaking Out

If you’re experiencing pain, swelling, or hard tissue near your surgical site after a BioZorb implant, you’re not alone. Across the country, women are coming forward with nearly identical stories—unexpected complications, ongoing discomfort, and no prior warning about the risks.

What makes this worse is that many women received BioZorb implants after surviving breast cancer. The device was supposed to help with healing—not lead to more pain, fear, and surgery. For many, the physical and emotional toll has been devastating.

Reports show that patients have experienced infections, painful scar tissue, hard masses forming around the implant, and long-term disfigurement. In some cases, doctors had to perform additional surgeries just to remove the device and treat resulting complications.

If this happened to you, it isn’t your fault—and it isn’t just bad luck. It may be the result of a defective product or a failure to warn. And you deserve to know the truth.

How Ferrer Poirot Feller Can Help

Taking on a medical device manufacturer isn’t easy, but that’s exactly what we’re here for. At Ferrer Poirot Feller, we’ve been helping injured patients hold corporations accountable for unsafe products for decades. When it comes to defective implants, we know what it takes to win.

Here’s how we support you:

• We investigate your surgery and implant records
• We gather documentation of your complications and follow-up care
• We work with medical experts who understand BioZorb failures
• We prepare and file your legal claim
• We handle all communication with the device maker and their lawyers

You don’t have to manage this process alone. Injury Lawyers Help Victims by taking care of everything, keeping you informed, and fighting for the compensation you deserve. That includes money for medical costs, pain and suffering, additional surgeries, and emotional trauma.

And remember, you pay nothing unless we win.

You’re Not Just Fighting Pain—You’re Holding the Manufacturer Accountable

BioZorb was marketed as a safe, innovative solution for post-surgical healing and radiation guidance. But patients were often not told about the risks of painful side effects, foreign body reactions, or hard tissue formation around the implant. Why do you need a lawyer? Because those risks weren’t always disclosed, and someone needs to hold the manufacturer accountable.

Manufacturers have a responsibility to fully test their products, monitor for complications, and warn patients and physicians about known risks. When they fail to do so, they must be held accountable.

At Ferrer Poirot Feller, we know what it takes to go up against major medical device companies. We don’t back down. We don’t get intimidated. And we don’t stop fighting until our clients get the justice they deserve.

You didn’t sign up for this pain. Let us help you stand up for what’s right.

What Is BioZorb and Why Was It Used?

BioZorb is a permanent surgical implant developed by Hologic, Inc. It was introduced as a 3D marker to help surgeons and radiation oncologists pinpoint the tumor site after a lumpectomy for breast cancer. The device consists of a spiral-shaped structure made of a resorbable material, with titanium clips that remain in the body permanently to assist in imaging and targeting radiation.

The implant was marketed as a tool to improve cosmetic outcomes, reduce the radiation field, and support tissue regrowth. However, many women who received BioZorb experienced the opposite—painful scar tissue, disfigurement, and ongoing inflammation.

While it was approved through the FDA’s 510(k) process, which allows quicker market access based on similarity to existing products, concerns have grown about the lack of clinical testing and long-term safety data. Despite being advertised as safe and supportive, BioZorb has led to serious complications for many patients—complications they were never warned about.

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What Are the Risks and Complications of BioZorb?

BioZorb was designed to remain in the body during recovery, with the expectation that its material would dissolve over time while the titanium clips stayed in place. Unfortunately, for many women, the device caused their bodies to react negatively, triggering immune responses, chronic inflammation, or tissue hardening. Choosing the right lawyer for you means finding someone who understands these complications and can build a strong case around the medical and legal details involved.

Common complications reported by patients include:

• Chronic or worsening pain
• Hard, visible masses at the implant site
• Infection requiring antibiotics or hospitalization
• Severe inflammation and foreign body reaction
• Breast distortion or asymmetry
• The need for revision or removal surgery

In some cases, surgeons were forced to remove the device months or years after implantation, often leading to additional scarring or emotional trauma. These risks were rarely discussed with patients beforehand, and that lack of warning may give rise to a legal claim.

Which Patients May Be Affected?

Most BioZorb implants were used in women who underwent breast-conserving surgery (lumpectomy) as part of their treatment for early-stage breast cancer. The device was promoted as a way to improve healing, enhance cosmetic results, and guide post-operative radiation therapy.

If you had breast surgery between 2012 and the present and were told a marker or surgical implant was used, you may have received BioZorb—especially if your surgeon discussed improved targeting or cosmetic benefits. Many patients weren’t told the specific brand name or long-term impact of the implant at the time.

You may be affected if:

• You had a lumpectomy and later experienced pain, swelling, or hard tissue buildup
• You had revision or removal surgery after the implant
• You developed an infection or other serious complication after breast surgery
• You were not warned about the risks of having a permanent or semi-permanent implant

If any of these apply to you, we can help confirm whether BioZorb was used—and whether you have grounds for a claim.

What Compensation May Be Available in a BioZorb Lawsuit?

If you were harmed by a BioZorb implant, you may be entitled to compensation for the physical, emotional, and financial impact it has had on your life. These lawsuits are not just about medical bills—they’re about accountability and helping you recover from a device that never should have caused harm.

Depending on your case, compensation may include:

• Medical expenses for follow-up care, antibiotics, or removal surgery
• Pain and suffering caused by chronic inflammation or disfigurement
• Lost income or time off work due to recovery
• Emotional distress, anxiety, or trauma
• Permanent changes in appearance or quality of life
• Punitive damages if the manufacturer is found to have acted recklessly

At Ferrer Poirot Feller, we work closely with medical experts, economists, and your healthcare team to fully document what you’ve been through. Our goal is to make sure no part of your suffering is overlooked—and that you receive the compensation you need to move forward.

Who Is Responsible for BioZorb Complications?

BioZorb is manufactured by Hologic, Inc., a medical device company that has marketed the implant as a safe, beneficial tool for breast cancer patients. However, many lawsuits allege that Hologic failed to adequately warn doctors and patients about the potential complications associated with the device.

Key legal claims may include:

• Failure to warn about the risks of chronic pain, inflammation, or hard tissue formation
• Inadequate safety testing before marketing the product
• Misleading marketing about cosmetic outcomes or radiation benefits
• Negligent design or manufacturing defects

Manufacturers of medical devices have a responsibility to ensure their products are both safe and effective. If they fail to do so—and people are harmed as a result—they can and should be held legally accountable.

We’ll investigate the full history of your case, identify the parties involved, and build a strong legal claim on your behalf. Lawyers can help maximize your compensation by uncovering every avenue of financial recovery, from medical bills to long-term emotional and physical impacts.

What to Expect When Filing a BioZorb Lawsuit

The process starts with a free consultation. During this conversation, we’ll ask about your surgery, the symptoms you’ve experienced, and whether you’ve needed additional treatment or removal of the implant. You don’t need to know whether BioZorb was used—we’ll help confirm that for you.

If we take your case, we’ll handle everything:

• Obtaining your medical and surgical records
• Confirming the use of a BioZorb implant
• Documenting your injuries and complications
• Consulting with surgeons and medical experts
• Filing the legal claim and negotiating a resolution

Most clients never have to go to court. But if the company refuses to offer a fair settlement, we’re fully prepared to fight for your rights at trial.

There are no upfront fees, and you won’t pay anything unless we win. You may be eligible for compensation if BioZorb caused complications like pain, infection, or the need for revision surgery. We’ll guide you every step of the way—with compassion, clarity, and real legal strength.

Contact Us for a Free Case Evaluation

If you experienced serious complications after receiving a BioZorb implant—whether it led to pain, infection, scarring, or revision surgery—you may have a legal right to compensation. You were never told this device could cause permanent harm. Now it’s time to get the answers and accountability you deserve.

At Ferrer Poirot Feller, we help people across the country take legal action against unsafe medical devices. We offer free, no-obligation consultations where we’ll listen to your story, review your case, and explain your legal options clearly and honestly.

You won’t pay anything unless we win your case.

Call us at (800) 210-8503 or contact us online to schedule your free case evaluation.

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