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Catheter Recalled Due to Increased Risk of Injury and Death The U.S. Food and Drug Administration (FDA) recently announced that Penumbra is recalling its JET 7 Reperfusion Catheter with Xtra Flex Technology due to the risks that it poses for causing serious injuries and even death in patients who use it. The catheter is typically used for removing clots in stroke patients, but the company (more...)

Power Morcellator Cancer Lawsuits Consolidated Into Multidistrict Litigation Power morcellators are medical devices that can perform hysterectomies and other medical procedures in a less invasive manner than traditional surgical methods. However, the device lost credibility when it was discovered it can significantly increase the chances of developing cancer in some women. Researchers found that when the morcellator is used, dormant cancerous cells can (more...)

Injuries, Deaths, and IVC Filter Lawsuits Prompt Investigation Companies that manufacture medical devices are required by law to ensure the safety and proper function of their products. However, an investigation has shown that C.R. Bard, Inc.—a medical device manufacturer—may have known about risks that its Inferior Vena Cava (IVC) filter posed to patients without taking corrective action. An IVC filter is a small (more...)

Cybersecurity Risks Present New Challenges for Medical Device Manufacturers Many manufacturers of medical devices now design products that can be integrated with wireless technology. While this can be convenient for sending and receiving data, the defective medical device lawyers at Ferrer, Poirot & Wansbrough explain this technology may also compromise the safety and security of the device. For example, infusion pumps deliver small amounts (more...)