As of October 2024, the status of the BioZorb litigation is drawing significant attention due to numerous ongoing legal claims and patient concerns. The October recall removed all unused BioZorb Markers from the market.
Hologic, the device’s manufacturer, stated the recall was a precaution to prevent further harm. If you are wondering what the status of the BioZorb implant lawsuit is, a Charlotte BioZorb implant lawsuit lawyer can help clarify legal options as the litigation continues to evolve.
Background of the BioZorb Implant Litigation
The BioZorb implant litigation has gained momentum in recent years due to allegations that the device caused significant injuries to patients. For those exploring legal options, consulting with a Charlotte mass tort lawyer can help provide clarity.
The U.S. Food & Drug Administration (FDA) issued a safety communication on October 25, 2024, from Hologic, Inc. It warned consumers not to use BioZorb Marker implantable radiographic marker devices after reports of serious complications.
Risk Factors and Complications
The BioZorb Marker, a small, coiled device with titanium clips, was designed to help locate tissue surrounding a tumor site during breast cancer treatment. While intended to dissolve over time, the titanium clips remain permanently in the body.
However, lawsuits allege the device caused injuries such as migration to other parts of the body, erosion through the skin, and fluid buildup (seroma), often requiring additional surgeries. Legal action began in November 2022 when lawsuits were filed in the United States District Court for the District of Massachusetts.
The litigation grew after Hologic issued a safety notification in February 2024, alerting healthcare providers about risks related to the device. The October 2024 recall followed reports of 399 complaints out of 91,531 devices distributed, including 188 injury-related complaints as of October 16, 2024.
Upcoming Trial
The bulk of BioZorb lawsuits are currently consolidated in the Massachusetts District Court under Judge Allison Burroughs. Plaintiffs claim the device is defective and that Hologic failed to warn about its risks adequately. The first trial, set for September 2025, could play a pivotal role in the outcome of future claims.
For a free legal consultation, call (877) 333-1000
How a BioZorb Implant Lawsuit Attorney Can Help
If you’ve experienced complications from a BioZorb implant, hiring a lawsuit attorney can provide the support and expertise needed to pursue justice and compensation.
Here’s how they can assist:
- Case evaluation: An attorney will review your medical records, symptoms, and the timeline of events to determine if your injuries, such as device migration, fluid buildup (seroma), or erosion, are linked to the BioZorb implant.
- Evidence collection: They will gather key evidence, including medical documentation, expert opinions, and reports of similar cases, to build a strong case on your behalf.
- Negotiation with defendants: A BioZorb lawsuit attorney will negotiate with Hologic, Inc. or their legal team to seek compensation for your medical bills, lost wages, pain, and suffering.
- Representation in court: If a settlement cannot be reached, your attorney will represent you in court, advocating for your rights and working toward the best possible outcome.
- Guidance through legal processes: Lawsuits can be overwhelming, but an attorney will handle legal filings, deadlines, and procedures, ensuring you stay informed and your case progresses smoothly.
For those in North Carolina, a Charlotte BioZorb implant lawsuit lawyer can provide personalized, local legal support tailored to your situation. With their help, you can focus on recovery while they fight to hold the manufacturer accountable.
Who Qualifies for a BioZorb Lawsuit?
Patients who have received a BioZorb implant and experienced complications may be eligible to file a lawsuit against the device’s manufacturer, Hologic, Inc. The following criteria must typically be met:
- BioZorb implant recipient: You must have received a BioZorb implant, typically used in breast cancer surgeries, as part of your treatment.
- Documented complications: You should have experienced specific injuries or complications linked to the device, such as device migration (movement to other parts of the body), fluid buildup (seroma), or erosion through the skin.
- Medical treatment related to the device: If the implant caused complications that required additional surgeries (e.g., removal of the device) or ongoing medical care, this strengthens your case.
The Importance of Medical Records and Proof
To file a successful claim, you must provide evidence that links your injuries to the BioZorb implant. This includes:
- Detailed medical records: Your healthcare records should show that a BioZorb implant was used during your treatment and document any complications or follow-up care related to the device.
- Proof of injuries: Photographs, imaging scans, surgical reports, and physician notes can help demonstrate the extent of your injuries.
- Timeline of events: A clear timeline showing when the implant was placed, when complications began, and what treatment was required is crucial for establishing a connection.
Click to contact our personal injury lawyers today
We Can Let You Know What the Status of the BioZorb Implant Litigation Is Throughout Your Case
The ongoing BioZorb implant litigation highlights the serious complications many patients have faced due to this medical device. For those who have suffered injuries, filing a lawsuit represents an opportunity to seek justice and compensation for the harm caused.
An experienced Charlotte mass tort lawyer can let you know what the status of the BioZorb implant litigation is throughout your case, ensuring you stay informed every step of the way.
If you or a loved one has been harmed by a BioZorb implant, don’t wait to take action. Contact DeMayo Law Offices today for a free case review.
Call or text (877) 333-1000 or complete a Free Case Evaluation form
