FDA Issues Early Alert on Automated Impella Controller Fixation Issue: What Patients and Hospitals Need to Know The U.S. Food and Drug Administration (FDA) has...
New Study Shows Promise for Early Detection of Pressure Injuries with MIMOSA Pro Device Hamilton Health Sciences (HHS) is reporting encouraging results from a pilot...
FDA Issues Class I Correction for mo-Vis R-net Wheelchair Joysticks Over Dangerous Firmware Error The U.S. Food and Drug Administration (FDA) has issued a Class...
BioZorb Cancer Implant Recall: Bloomberg Exposes Patient Harm, FDA Failures, and Corporate Negligence When Bloomberg published its September 3, 2025 feature on the BioZorb cancer...
Tandem Diabetes Care Issues Recall of t:slim X2 Insulin Pumps Tandem Diabetes Care, Inc. has announced a voluntary medical device correction involving its t:slim X2...
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...
Medtronic's Left Heart Vent Catheter Recall: A Wake-Up Call for Medical Device Quality At Ketterer, Browne & Davani (KBD) Attorneys, we closely track issues involving...
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...
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...
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...
