BioZorb® Lawsuit

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BioZorb® Markers have been recalled after some patients reported serious injuries caused by the device breaking through their skin or migrating inside the body. By filing a BioZorb lawsuit, victims can seek compensation for their medical bills and hold the manufacturer of this device accountable. See if a top lawyer may be able to fight hard for everything you deserve.

Rae Theodore

Fact-Checked and Legally Reviewed by: Rae Theodore

Last updated:

Understanding the BioZorb Titanium Breast Marker Lawsuit

BioZorb Markers are implantable devices used in patients getting treatment for breast cancer to mark the site of the tumor removal.

They are made of two parts: a metal component that’s permanent and a plastic component that’s supposed to dissolve over time.

In October 2024, Hologic® Inc., BioZorb’s manufacturer, announced a voluntary recall of all lots of the unused markers. The U.S. Food and Drug Administration (FDA) identified the BioZorb recall as a Class 1 recall, which is the most serious type.

The recall was issued due to reports of serious health problems, including the device moving out of position or eroding and breaking through the skin. In some cases, patients may need surgery to remove the BioZorb Marker.

Now, victims are taking legal action to hold Hologic accountable and pursue compensation for medical expenses, pain and suffering, and more.

LawFirm.com has partnered with experienced product liability attorneys who have recovered over $1.6 billion for patients harmed by dangerous medical devices and drugs.

Am I Eligible to File a BioZorb Marker Lawsuit?

You may qualify to file a BioZorb Marker lawsuit if you or a loved one:

  • Received a BioZorb Marker or BioZorb LP Marker implant
  • Suffered complications like device migration or erosion
  • Underwent surgery or was told surgery was needed

Patients only have a limited time to file a BioZorb recall lawsuit due to laws called statutes of limitations. The BioZorb lawsuit statute of limitations varies by state but can be as short as 1 year, depending on where you live.

A BioZorb lawyer can explain the deadline that applies in your case and act quickly so you don’t miss out on your window of opportunity.

BioZorb Complications

While meant to improve outcomes for breast cancer patients, some of those who received a BioZorb implant have reported serious complications and adverse events.

BioZorb Marker complications include:

  • Device erosion: The breast biopsy marker can break through soft tissue, leading to exposed skin and increasing the risk of infection.
  • Device migration: The BioZorb implant may shift from its original position, damaging nearby tissue or causing other complications.
  • Fluid buildup (seroma): Excess fluid can collect around the implant and result in swelling and discomfort.
  • Infections: If bacteria grows around the implant site, it can lead to swelling, fever, or other symptoms.
  • Persistent pain: Some patients experience ongoing pain and irritation, even months after they were implanted with the device.

Hologic reports that, of the 91,521 BioZorb Markers distributed since 2015, there have been 399 complaints with 188 cases linked to serious complications like pain, infection, device migration, and erosion.

If you’re experiencing any BioZorb breast biopsy marker side effects, contact your doctor. In some cases, patients may need surgery to remove the breast biopsy marker or other additional medical treatments to help with BioZorb complications.

Compensation from a BioZorb lawsuit can help you cover any future medical procedures you may need and more.

Steps to File a BioZorb Recall Lawsuit

LawFirm.com works with BioZorb recall lawyers who understand the emotional distress of having a defective medical device implanted in your body. They strive to make the legal process as easy and stress-free as possible.

With your legal team fighting for the money you deserve, you’ll be able to focus on your health.

The basic steps involved in filing a BioZorb lawsuit include:

  1. Getting a free case review: A free consultation with an experienced lawyer allows you to find out about your legal options without spending a dime.
  2. Gathering evidence: Your legal team will collect evidence, like your medical records and information about your BioZorb breast biopsy marker, to create a strong case.
  3. Filing your BioZorb lawsuit: Your attorney will file your BioZorb Marker lawsuit in the proper court before any legal deadlines.
  4. Accessing compensation: Money from a BioZorb lawsuit settlement can ease financial worries, so your team will work to secure the compensation you deserve as quickly as possible.

If a BioZorb settlement is unable to be reached, your lawyer will be prepared to argue your case in court and fight for a trial verdict that provides maximum compensation.

LawFirm.com works with Biozorb lawyers who have decades of experience handling complex medical device recall cases and securing justice for clients.

Get Help From a BioZorb Recall Lawyer

Medical device makers are required to design products that are safe for use and warn patients of any potential health risks.

A BioZorb lawsuit allows those who’ve been harmed to hold Hologic accountable for its negligence.

The BioZorb lawyers that LawFirm.com works with can even the playing field for victims by standing up to this multi-billion dollar company on their behalf.

The product liability lawyers in our network:

  • Are leaders in medical device recall litigation
  • Can help BioZorb victims in all 50 states
  • Never charge any upfront costs or hourly fees

Our legal partners have secured more than $1.6 billion for patients harmed by defective medical devices and drugs.

BioZorb Lawsuit FAQs

The breast biopsy marker lawsuit involves claims that the BioZorb Marker failed to resorb as intended, causing serious injuries.

Some patients, for example, have reported that the device migrated inside their body or broke through the skin.

BioZorb implant lawsuits claim that Hologic, Inc., the manufacturer of the titanium breast marker, failed to adequately warn about these and other risks, preventing patients from making informed decisions about their health.

A Hologic lawsuit is a way for victims to hold the company accountable and seek compensation for their medical bills, pain and suffering, and more.

Individual lawsuits are currently being filed, but a BioZorb class action lawsuit may be created in the near future as the claims against the product’s manufacturer mount.

Over 100 victims have filed BioZorb lawsuits in Massachusetts, where the device’s manufacturer, Hologic, is headquartered. Thousands of women have been implanted with the BioZorb Marker, so that number is likely to increase.

BioZorb is intended to dissolve inside a patient’s body in 1 year or more. However, in some cases, BioZorb devices have failed to dissolve, leading to infections, chronic pain, and other serious complications.

Some patients have fought back by filing BioZorb lawsuits seeking compensation for surgeries and other medical treatments they’ve needed as a result of the recalled medical device.

The side effects of a titanium marker in the breast range from pain at the marker insertion site to the formation of scar tissue near the marker.

However, a titanium breast marker called the BioZorb has been linked to more serious issues.

BioZorb titanium breast marker problems include:

  • Device erosion (breaking through the skin)
  • Device migration (traveling inside the body)
  • Discomfort around the device
  • Fluid buildup
  • Infections
  • Sensations of the device being present in the breast

Patients may need additional surgeries to remove their BioZorb Markers or other treatments due to these complications.

Yes, it’s possible that a marker in the breast after a biopsy could cause pain years later.

While these devices are meant to dissolve over time, some patients with the BioZorbs have reported severe pain afterward and even needed to have them surgically removed.

After receiving numerous complaints, the manufacturer recalled unused BioZorb Markers and informed patients and health care providers of the potential risks associated with the marker.

Compensation from a BioZorb recall lawsuit can help patients pay for their medical bills and more.

Rae Theodore

Fact-Checked and Legally Reviewed by: Rae Theodore

Rae Theodore is a writer and editor with more than 30 years of experience in legal publishing. She earned a bachelor’s degree in English from Pennsylvania State University.

Last modified:
  1. HealthCentral. (2023, October 2). “Is it Safe to Have a Titanium Marker in My Breast?” Retrieved from https://www.healthcentral.com/article/the-titanium-marker-should-you-worry.
  2. Hologic. (2024, October 24). “URGENT: MEDICAL DEVICE RECALL: BioZorb® 3D Bioabsorbable Marker.” Retrieved from https://www.hologic.com/biozorb-3d-bioabsorbable-marker/important-safety-information.
  3. Sokolove Law. (2025, January 2). “BioZorb Lawsuit.” Retrieved from https://www.sokolovelaw.com/product-liability/medical-devices/biozorb-marker/.
  4. Targeted Oncology. (2024, October 30). “FDA Issues Warning on BioZorb Markers After Recall Due to Patient Complications.” Retrieved from https://www.targetedonc.com/view/fda-issues-warning-on-biozorb-markers-after-recall-due-to-patient-complications.
  5. U.S. Food and Drug Administration. (2024, December 18). “Update: Do Not Use BioZorb Marker Implantable Radiographic Marker Devices: FDA Safety Communication.” Retrieved from https://www.fda.gov/medical-devices/safety-communications/update-do-not-use-biozorb-marker-implantable-radiographic-marker-devices-fda-safety-communication.