The Nightmare of Mesh Removal

The Nightmare of Mesh Removal: What Patients Need to Know At KBD Attorneys, we have been following the growing crisis surrounding surgical mesh implants—devices often...

Different Types of Transvaginal Mesh

Understanding the Different Types of Transvaginal Mesh and How KBD Attorneys Can Help Transvaginal mesh (TVM) devices were introduced to treat conditions like pelvic organ...

WATCHMAN Access System Safety Issue

Early Alert: WATCHMAN Access System Safety Issue and the Importance of Medical Device Recalls Medical device safety is a critical concern for healthcare providers and...

Philips Respironics BiPAP Ventilators Recall

FDA Issues Most Serious Type of Recall for Philips Respironics BiPAP Ventilators — Lives at Risk Without Urgent Action The U.S. Food and Drug Administration...

Urgent Recall: HeartSine Samaritan Defibrillators

HeartSine Samaritan Defibrillators May Fail When Lives Depend on Them Defective AED devices recalled due to dangerous circuit issue – KBD Attorneys is investigating potential...

Update: BD Alaris™ Infusion Pump Has Legacy Part Failures

Update: BD Alaris™ Infusion Pump Recall Expands Due to Legacy Part Failures KBD Attorneys Continues to Investigate Defective Medical Device Injuries Linked to BD’s Alaris™...

Cook Medical Angiographic Catheter Recall

Cook Medical Angiographic Catheter Recall At KBD Attorneys, we regularly investigate product recalls involving medical devices, especially when those products place patients at risk of...

Latest Abbott HeartMate Recall the Most Serious Yet

FDA Deems Latest Abbott HeartMate Recall the Most Serious Yet In another alarming development for patients relying on mechanical heart support, the FDA has classified...

FDA’s Controversial Approval of Humacyte’s Artificial Blood Vessel

FDA’s Controversial Approval of Humacyte’s Artificial Blood Vessel In December, the U.S. Food and Drug Administration (FDA) approved a first-of-its-kind artificial blood vessel—Symvess—created by Humacyte...

Philips Removes and Discontinues Distribution of Tack Endovascular System

Philips Removes and Discontinues Distribution of Tack Endovascular System Due to User Challenges The recent recall of the Tack Endovascular System by Philips has raised...

Defective Medical Device

The Nightmare of Mesh Removal

Different Types of Transvaginal Mesh

WATCHMAN Access System Safety Issue

Philips Respironics BiPAP Ventilators Recall

Urgent Recall: HeartSine Samaritan Defibrillators

Update: BD Alaris™ Infusion Pump Has Legacy Part Failures

Cook Medical Angiographic Catheter Recall

Latest Abbott HeartMate Recall the Most Serious Yet

FDA’s Controversial Approval of Humacyte’s Artificial Blood Vessel

Philips Removes and Discontinues Distribution of Tack Endovascular System

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