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...
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...
At KBD Attorneys, we have been following the growing crisis surrounding surgical mesh implants—devices often used to treat conditions like hernias, pelvic organ prolapse, or...
At Ketterer, Browne & Davani (KBD) Attorneys, we closely track issues involving medical device safety and accountability. In fact, we have written about Medtronic before,...
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...
Understanding IVC Filter Lawsuits: What You Need to Know Medical devices, while many save lives, some can lead to complications that have lasting effects. One...