Injured by a Medical Device? Here’s What You Should Know.
Medical devices are specifically designed for medical purposes and are used to diagnose, treat or monitor a patient suffering from a particular disease or disability and improve the […]
FDA: Recall Issued for Abbott NC Trek RX and NC Traveler RX Coronary Dilatation Catheters
Abbott Vascular is recalling NC Trek RX Coronary Dilatation Catheter and NC Traveler RX Coronary Dilatation Catheters because some balloons from the impacted lots may not deflate as […]
FDA: Recall Issued for Medtronic MiniMed Insulin Pumps
On February 12, the Food and Drug Administration (FDA) announced that Medtronic has issued a recall on certain models of its MiniMed 600 Series Insulin Pumps. The recalled […]
FDA: Medtronic Pacemaker Battery Depletion May Lead to Loss of Function
On May 7, 2019, the U.S. Food and Drug Administration (FDA) issued a safety communication about issues with certain Medtronic implantable pacemakers or cardiac resynchronization therapy pacemakers (CRT-Ps). […]
Report: Bayer to Discontinue Essure After FDA Restrictions, Decline in Sales
Attorneys are currently investigating allegations of adverse health events associated with a permanent form of birth control known as Essure. After continued monitoring and possible penalties imposed by […]
Study: Magnetic Growing Rods Could Release Metal Ions into Soft Tissues
Researchers reportedly indicate that metal ions released from traditional and magnetically controlled growing rods can potentially “cause localized debris and distribute systemically to settle on distant organs.” Magnetically […]
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FDA: Abbott Issues Voluntary Recall of Coronary Catheters
Abbott Vascular has initiated a voluntary coronary catheter recall for specific lots of three catheters manufactured and distributed between 2015 and 2017. According to the U.S. Food and […]
Report: FDA Warns St. Jude for Failing to Investigate Defibrillator Problems
The U.S. Food and Drug Administration (FDA) has reportedly sent a St. Jude defibrillator warning letter accusing the device manufacturer of failing to adequately investigate problems related to […]
Report: Nationwide EpiPen Recall Issued Due to Potential Device Failure
A nationwide Mylan EpiPen recall has been issued by Meridian Medical Technologies for 13 lots of Mylan’s EpiPen and EpiPen Jr Auto-Injectors used for the emergency treatment of severe […]
FDA: Philips Healthcare Recalls HeartStart MRx Monitor/Defibrillator
Philips Healthcare has initiated a recall for the HeartStart MRx Monitor/Defibrillator because of issues with the electrical and battery connections that could prevent the device from powering up, charging […]
Lawsuit: Leaking Breast Implants Led to Serious Health Problems
A defective breast implant attorney notes that a lawsuit alleges silicone breast implants sold by a Johnson & Johnson subsidiary may leak and lead to serious problems for […]
Greatbatch Medical Recalls Standard Offset Cup Impactors
A Greatbatch Standard Offset Cup Impactor recall has been initiated due to failed sterilization testing of the reusable surgical devices. Devices that have failed such testing can potentially […]
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Centurion Announces Multi-Med Single Lumen Catheter Recall
A Centurion Multi-Med Catheter recall has been initiated because the catheters have a potential for excess material to remain at the tip of the catheter, possibly leading to […]
Federal Jury Awards Over $1 Billion in DePuy Pinnacle Case
A DePuy Pinnacle hip implant attorney notes that a jury awarded over $1 billion to six plaintiffs in a third case against multinational medical device manufacturer Johnson & […]
Lawsuit: Ventralex Hernia Patch Incompatible with Human Tissue
A Ventralex Hernia Patch lawyer notes that a lawsuit alleges the devices may be made of materials biologically incompatible with human tissue, potentially leading to severe health complications. […]