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FDA Recalls HeartMate 3 LV Assist Device

In May 2018, less than a year after approval, the Federal Food and Drug Administration (FDA) issued a Class I recall on HeartMate 3, a medical device which is inserted into patients to treat heart failure. The device assists in pumping blood in the left ventricle of the heart of patents who are at risk » Read More

Essure Complications and Medical Device Lawsuits

In 2002, the Federal Food and Drug Administration (FDA) approved Essure. Essure was designed as a medical device to prevent pregnancies in women. Women are inserted with two of the devices, which resemble a coil, one in each fallopian tube, to assist the body in creating a natural blockage in the tubes in order to » Read More