We Can Help
Why Clients Choose Bernheim Kelley
Not every patient will qualify for a BioZorb lawsuit. In general, claims are being evaluated for patients who experienced complications after implantation that resulted in revision surgery, removal of the BioZorb device, or other significant medical treatment.
If you're unsure whether you qualify, let us review your medical records. Your consultation is free, and there is no obligation.
- Focused Experience in Complex Medical Device Litigation — we represent individuals injured by dangerous medical devices and understand the medical, scientific, and legal issues involved.
- No Fee Unless We Win — you pay nothing upfront; we advance the costs of pursuing your case and only receive a fee if we recover compensation for you.
- Free, No-Obligation Case Review — speak directly with our legal team about what happened, whether you may qualify, and what to expect.
- Thorough Investigation — we obtain and review your medical records, operative reports, pathology records, and other evidence to build the strongest case possible.
- Personalized Representation — direct communication, honest answers, and individualized attention throughout your case.
The BioZorb® Lawsuit
Implanted During Breast-Conserving Surgery
The BioZorb® marker is a breast tissue marker implanted during breast-conserving surgery (a lumpectomy), manufactured by Hologic, Inc.
The lawsuits allege that some patients experienced serious complications following implantation that required additional medical treatment or corrective surgery. If you experienced complications after receiving a BioZorb implant, you may have legal options — contact us today for a free, confidential case evaluation.
Do You Qualify?
Alleged Complications
The lawsuits allege complications including the following — and claims are being evaluated where complications led to further treatment or surgery:
Pain
Ongoing or severe pain after implantation of the tissue marker.
Infection
Infection at or around the implant site following surgery.
Device Migration
The BioZorb device moving from where it was implanted.
Erosion
The device eroding through tissue or skin after implantation.
Delayed Healing
The surgical site failing to heal properly or on schedule.
Inflammation
Inflammation and other adverse events after implantation.
Revision Surgery
Complications that resulted in additional corrective surgery.
Device Removal
Complications that required the BioZorb device to be removed.
Other Significant Treatment
Other significant medical treatment made necessary by complications.
Don't Wait to Protect Your Rights
Time Is Limited to File
Every state has a deadline — called the statute of limitations — for filing a lawsuit. Waiting too long could prevent you from pursuing compensation. Contact us as soon as possible so we can evaluate your claim and help protect your legal rights.
Your Case Review
What We Look At
Call Bernheim Kelley Injury Lawyers today at 617-468-5342 — our team is available to answer your questions, discuss your legal options, and provide a free, no-obligation case evaluation. Your free review covers:
- Who was implanted — you, or a loved one.
- When the BioZorb device was implanted — 2026, 2025, 2024, 2023, 2022, or before 2022.
- What happened afterward — complications, and whether revision surgery or removal has happened, or your doctor has recommended it.
- Where it happened — the state where your surgery took place.
- When to talk — after you submit, you can pick a time (morning, afternoon, or evening) to speak with our team.
Our Offices
Florida — Fort Lauderdale · Miami · Jacksonville · Fort Myers · Starke
Massachusetts — Boston · Plymouth
Tennessee — Nashville