Miller Mikro-Tip Angiographic Catheters Recalled in California, District of Columbia, Massachusetts, Michigan, Minnesota, New York, and Pennsylvania
On April 1, 2011, the U.S. Food and Drug Administration (FDA) posted that the Miller Human Use High Injection Angiographic Catheters were recalled for potential debris in the catheter. The particles or debris in the catheter could become dislodged, travel throughout the body and cause an emboli or obstruction in blood vessels, tissue, organs or limbs. Any disruption in blood flow to vital organs can cause a heart attack or myocardial infarction, stroke, limb ischemia, blindness, liver or kidney failure, or even death.
This type of catheter is used in interventional radiology and interventional cardiology studies. It not only is used to measure pressure within the blood vessels, it can also be used to administer or inject radiopaque or contrast material into the body for better view of the blood vessels.
Miller contacted hospital risk managers, radiologists, cardiologists and other healthcare providers notifying them of the recall.
As a physician and experienced Philadelphia defective product lawyer, I know firsthand the catastrophic injuries or wrongful deaths that can come from dangerous, faulty or recalled medical devices. Since 1958, the experienced medical and legal teams at The Beasley Firm have gone up against some the most prominent or powerful medical equipment manufacturers and won.
Our medical experience and legal knowledge has provided our clients with thousands of awards in the seven, eight or nine figure range. To date, we have had billions awarded on behalf of our injured clients. Our medical and legal experience will not only help you to try and obtain compensation for the thousands of dollars in medical bills you have been forced to pay, but also the income you have lost from not being able to work. We are also committed to helping you receive compensation for the severe pain and suffering you and a loved one have been through as a result of the careless and reckless behavior of companies like Miller who defectively designed, manufactured, or quickly put faulty and dangerous products out on the market. We believe that these manufacturers, big businesses, and corporations should be held accountable for their wrongdoings.
Our record of success speaks for itself. If you or a loved one has been injured due to a defective product, contact one of our experienced Pennsylvania medical equipment recall attorneys at (888) 823-5291. As always, we offer a zero fee guarantee which means that if we don't make a recovery on your behalf, you don't owe us a dime. We always offer a free, no obligation consultation.