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Exactech Hip Recall and Litigation – Connexion GXL

Another Artificial Hip Failure The attorneys at KBA have seen this before, hip replacement failures. Artificial hips are a kind of medical device. They sometimes fail. Patients who...
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Research Suggests Vaping-Related Lung Disease May Be Caused by Chemical Exposure

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...
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Knee Implant Failures and Bone Cement

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...
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Knee Implant Failures May Be Due to Bone Cement

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...
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FDA Issues Class I Recall For Ethicon’s Circular Surgical Staplers

KBA previously noted problems with surgical staplers. Once again, defective surgical staplers are in the news. Today, following the FDA’s March 2019 warnings to surgeons...
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Surgical Staplers & Staples Found Unsafe

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...
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FDA Warns Breast Implant Manufacturers

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...
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Lime Scooter Defects Cause Injuries

Lime, a scooter-based ride-sharing app, has recently run into trouble with their software and hardware which has been making their scooters malfunction and cause injuries...
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Robotically-Assisted Surgical Devices and Women’s Health

Safety communication has recently been issued by the Food and Drug Administration (FDA) involving the effectiveness and safety of cancer procedures utilizing robotically-assisted surgical devices....
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FDA Recalls CoaguChek XS PT Test Strips

The FDA has announced a Class I recall on Roche’s CoaguChek XS PT Test Strips that were manufactured from January 12, 2018, to October 29,...
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