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J&J Remove LINX Reflux Fom Market

Johnson & Johnson to Withdraw LINX Reflux Management Device from Markets Outside the U.S. Patients living with gastroesophageal reflux disease (GERD) often struggle with daily...
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Recall of Olympus FLEX Needles

Olympus Issues Voluntary Recall for ViziShot 2 FLEX Needles: What Patients & Providers Should Know On September 19, 2025, Olympus Corporation announced a global voluntary...
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Burn Injuries from Oil Field Explosions

Burn injuries are some of the most serious and life-altering injuries a person can experience. While burns can occur in many settings—such as home fires,...
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Boston Scientific Transvaginal Mesh Lawsuit

Boston Scientific Transvaginal Mesh Lawsuit: What You Need to Know Ketterer, Browne & Davini, LLC is currently representing a plaintiff in a lawsuit against Boston...
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Filing A Claim For A Hit-And-Run Witness

Being present at a hit-and-run in any capacity can be unsettling, but those who witness these incidents may not realize they play a vital role....
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Automated Impella Controller Fixation Issue

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...
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New Implant Helps Stabilize Blood Pressure in Spinal Cord Injuries

New Implantable Device Offers Breakthrough in Stabilizing Blood Pressure for Spinal Cord Injury Patients For people living with spinal cord injuries (SCI), the challenges extend...
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Nursing Home Lawsuits Surge in North Carolina

Nursing Home Lawsuits Surge in North Carolina Amid Claims of Neglect and Profit-Driven Care The nursing home industry is once again under a harsh spotlight,...
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Maryland Nursing Home Inspections: Why Timely Checks Matter for Resident Safety

Maryland Nursing Home Inspections: Why Timely Checks Matter for Resident Safety Ensuring Quality Care: The Importance of Timely Nursing Home Inspections In Maryland, a recent...
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FDA Updates Boston Scientific Defibrillator Lead Recall After 16 Deaths

FDA Updates Boston Scientific Defibrillation Lead Recall After 16 Deaths Reported The U.S. Food and Drug Administration (FDA) has issued a correction notice related to...
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