National Personal Injury and Mass Torts Law - Parker Waichman LLP
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Medtronic Defibrillator Lawsuits - Parker Waichman LLP
Medtronic Recalls Series of Medtronic Cardiac Resynchronization Therapy with Defibrillation (CRT-Ds) and Implantable Cardiovert-Defibrillators (ICDs) According to the United States Food and Drug Administration, the medical device manufacturer Medtronic has issued a recall of some of its defibrillator products.
Medtronic Recalls Nearly 100,000 Pacemakers for Battery Problems
Medtronic has issued a recall for about 96,800 InSync III pacemakers because of a battery defect that may prevent the device from operating properly, endangering the patient. The recall covers three different pacemaker models. In a letter to doctors, Medtronic wrote that 30 of the devices have been demonstrated to…
Medtronic Insulin Pump Battery Malfunction Lawsuit Lawyers
Medtronic initially alerted its customers to this issue in July 2024. However, the situation has escalated, and the FDA’s classification of the recall underscores the gravity of the problem. In response, Medtronic has issued guidance for users, urging them to monitor their insulin pumps closely for any signs of decreased battery life or ...
Covidien/Medtronic Hernia Mesh Lawsuits - Parker Waichman LLP
Call Parker Waichman LLP to Discuss Your Covidien/Medtronic Hernia Mesh Claim. Time could be running to file your potential claim, so do not delay in contacting us to begin your case investigation. Contact Parker Waichman LLP today for your free case consultation by calling 1-800-YOURLAWYER (1-800-968-7529) or by filling out our online form.
Medtronic Cardiac Defibrillator Lawsuit Lawyers
Contact a Medtronic Cardiac Defibrillator Lawsuit Lawyer Today for a Free Consultation. If you or a member of your family has sustained injuries because of a Medtronic Cardiac Defibrillator, it may be time to discuss your situation with a qualified lawyer who handles defective drug and medical device cases on a regular basis.
Medtronic HeartWare HVAD System Lawsuit Lawyers
Medtronic voluntarily recalled the HeartWare HVAD System when it discovered that interruptions in the electrical connection of the device have caused the device to stop working suddenly. The reason for such interruptions is the development of oxidation along the connecting surfaces between the controller’s power source socket and the power ...
Medtronic - Parker Waichman LLP
Medtronic As one of the nation’s premier personal injury and mass tort law firms, we are capable of successfully handling all types of cases. If you or a loved one are injured due to the negligence of another, there is no...
Medtronic MindFrame Capture LLP Revascularization Device …
The Medtronic device uses a wire material that has shown that it could break or become detached from the device and remain in the patient’s bloodstream. If this occurs, the device, or the physician’s efforts to remove the device, could cause injuries to the patient, including “bleeding, additional blockage of blood vessels, more severe ...
Medtronic’s StealthStation S8 Lawsuit Lawyers - yourlawyer.com
This misplacement can lead to serious permanent injuries such as brain, nerve, or cerebrovascular damage, abnormal brain, spine, or muscle functions, paralysis, or even death. The U.S. Food and Drug Administration (FDA) has issued a Class I recall, the most serious type of recall, for Medtronic’s StealthStation S8 application. This software, crucial for locating …