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...
Philips Cardiac Telemetry Recall: Updated FDA Classification and What It Means for Patients The FDA escalated its recall classification for Philips’ outpatient cardiac telemetry system...
KBD Attorneys litigates product liability cases. As a product liability lawyer, we advocate for people when a product injures them. We learn about people in...
Another Artificial Hip Failure The attorneys at KBD have seen this before, hip replacement failures. Artificial hips are a kind of medical device. They sometimes fail. Patients who...
One group of authors define e-cigarettes as follows, "E-cigarettes are battery-operated devices that heat a liquid and deliver an aerosolized product to the user." Another...
What is bone cement and how it is used? Patients' medical conditions sometimes require the implantation of a medical device to replace damaged bone. One...
Patients who have had a knee replacement and a knee implant failure may be suffering due to high-viscosity bone cement failures. Traumatic injuries, aging, and...
KBD previously noted problems with surgical staplers. Once again, defective surgical staplers are in the news. Following the FDA’s March 2019 warnings to surgeons about...
Recent reports of defective surgical staplers and staples have patients, doctors, and the U.S. Food and Drug Administration (FDA) concerned. What Are Surgical Staplers? Surgical...
Two breast implant manufacturers were recently issued warning letters from the U.S. Food and Drug Administration (FDA) because they did not comply with the requirements...
