For many women undergoing breast cancer treatment, the BioZorb implant was presented as a tool to aid recovery. This small, coil-shaped surgical device is designed to mark the area where a tumor was removed during a lumpectomy, helping guide future radiation therapy and provide internal support as the body heals.
But for a growing number of patients, BioZorb hasn’t been part of healing—it’s been the source of new and painful complications.
What Is the Problem With BioZorb?
Patients and surgeons across the country are reporting serious long-term issues related to the BioZorb implant, including:
- Chronic pain and inflammation
- Scarring and disfigurement
- Device migration
- Need for additional surgeries to remove the implant
In many cases, patients were never told that the device might remain in the body for years—or indefinitely. Others were told it would be fully absorbed, only to discover years later that it hadn’t.
Importantly, the device was the subject of a Class I recall by the U.S. Food & Drug Administration, the most serious type of recall, due to the potential for serious injury. Hologic, the manufacturer, instructed health-care providers to stop using all remaining BioZorb units, quarantine unused devices, and return them. The recall underscores the severity of the risks and the recognition that the device could cause harm if implanted, further supporting plaintiffs’ claims of inadequate warning and defective design.
The Legal Argument: Failure to Warn and Defective Design
Emerging lawsuits allege that the manufacturers of BioZorb failed to adequately warn patients and physicians about the risks associated with the implant. They also raise questions about the device’s design, safety, and long-term compatibility with the body.
At the heart of this litigation is a simple principle: patients have a right to know what is being placed in their bodies and what risks come with it.
Who May Qualify to File a BioZorb Lawsuit?
You may be eligible to file a claim if you:
- Received a BioZorb implant after a lumpectomy
- Experienced complications such as pain, scarring, disfigurement, or required additional surgery
- Were not fully informed of the risks associated with the device
Even if your surgery was several years ago, you may still have a claim depending on your medical history and the symptoms you’ve experienced.
Why HGD Is Taking Action
At HGD, we’ve built a reputation for advocating fiercely and compassionately for those harmed by defective medical devices. We understand that for breast cancer survivors, this isn’t just a medical issue—it’s emotional, personal, and often deeply frustrating.
Our approach is simple:
- We listen to your story and evaluate your case with care
- We work with medical experts to build strong, fact-based claims
- We walk with you every step of the way, keeping the process transparent and focused on your well-being
If You’ve Been Affected by a BioZorb Implant, You’re Not Alone
The BioZorb lawsuits are just beginning to gain momentum. If you believe the implant has caused you harm, now is the time to explore your legal options.
HGD is here to help you find answers, accountability, and a path forward.
Reach out today for a free and confidential consultation.
