Spotlight on BioZorb Recall: What You Need to Know

Jinks Crow is committed to keeping you informed with timely, meaningful updates that may impact health and safety. Recent investigative reporting from Bloomberg has shed new light on the recall of BioZorb, a medical device once marketed as a cutting-edge tool for breast cancer treatment. Read our summary of both articles below.

What is BioZorb?

BioZorb is a bioabsorbable marker coil implanted during breast-conserving surgery. It was designed to help doctors target radiation therapy more precisely and to provide cosmetic support as tissue healed. The device was marketed as innovative and widely adopted across the U.S., often presented as an advancement for breast cancer patients.

Why Was BioZorb Recalled?

In 2024, the FDA issued warnings that BioZorb could cause serious complications including chronic pain, infections, device migration, and even risk of death. Following these warnings, the manufacturer withdrew the product from the market.

For many patients, however, the recall came too late. Reports surfaced of women experiencing lasting harm after implantation, ranging from repeat surgeries to long-term physical and emotional trauma.

Bloomberg’s Findings

According to Bloomberg’s reporting (feature article and newsletter summary), the story goes deeper:

• Complaints were minimized: Internal concerns and patient complaints were allegedly downplayed while sales continued.

• Profits over patients: Despite knowledge of complications, the device was kept on the market and promoted to physicians.

• Regulatory blind spots: The case underscores broader weaknesses in how medical devices are approved, monitored, and recalled in the U.S.

What This Recall Means for BioZorb Patients

If you or a loved one received a BioZorb implant, here are key considerations:

1. Monitor your health closely. Stay alert for symptoms such as pain, swelling, infections, or other unusual changes, and share them with your healthcare provider immediately.

2. Consult with your doctor. Ask whether BioZorb may be affecting your recovery and what options are available if complications arise.

3. Understand your legal rights. Patients harmed by defective devices may be entitled to compensation for medical costs, pain and suffering, or corrective procedures. Taking action also helps ensure accountability for corporations that put profits ahead of safety.

   
   

The BioZorb recall underscores a troubling reality: medical devices meant to aid healing can sometimes cause harm when oversight fails and transparency is lacking. Patients deserve to be protected, not placed at risk.

At Jinks Crow, we stand with those who have been injured by unsafe products. If you are experiencing complications from a BioZorb implant, know that you are not alone. Contact us today for a free consultation.

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For more details, see Bloomberg’s full reporting (subscription required):

• BioZorb Recall Feature

• Buried Complaints Newsletter, Sept. 5, 2025

Note: This blog summarizes Bloomberg’s reporting in our own words for informational purposes. Original articles may require a subscription.