
Medical Device Failure
The BioZorb® 3D Bioabsorbable Marker was implanted in women who had a lumpectomy procedure. The device has been linked to a variety of complications for many patients, including erosion of the device (coming through the skin) and migration (movement of the device from its original position). These complications have caused infection, pain and other health concerns that have demanded additional medical treatment. If you or any of your loved ones have experienced complications after a BioZorb® implant, you may qualify for compensation that can help you recover lost wages, medical costs and a judgement for your pain and suffering.
KBD Attorneys helps clients navigate the often confusing and overwhelming world of litigation and brings you justice and compensation. BioZorb lawsuits are time-sensitive and working quickly is important. Contacting an attorney as soon as possible can help you strengthen your claim and get the justice you deserve.
Important Updates
2012 (February): Device leared by the United States Food and
Drug Administration
2024 (February): U.S. Food and Drug Administration issued a Safety Communication regarding BioZorb Markers.
2024 (March): FDA Class I Recall of BioZorb Marker.. Pursuant to FDA direction, Hologic sent an Important Medical Device Safety Notification to affected customers.
2024 (May): FDA gives the most serious class of recall (Class I) to Hologic’s communications to its customers.
2024 (December): FDA sent a Warning Letter to Hologic, stating that the inspection revealed the BioZorb devices “are not in conformity with the current good manufacturing practice requirements in the Code of Federal Regulations (CFR)".

What You Can Expect With Our Experienced Team?
What You Can Recover Compensation For In Your Case?

Proving neglect with medical devices takes experience, speed and attention to the specific details needed for such a lawsuit. How can we help you prove you succeed in your medical device lawsuit? Our experienced team works to:





