MindFrameCapture LP Revascularization Device Lawyer
At Myers & Flowers, we have represented thousands of patients in faulty medical device cases. We help our clients navigate the legal system if a loved one was injured or died after a surgeon inserted a MindFrameCapture LP Revascularization Device that failed during an attempt to retrieve a blood clot.
While many thousands of procedures are performed every year to retrieve blood clots from patients suffering a stroke, 529 of the MindFrameCapture LP Revascularization Device devices have been recalled due to the risk of device failure. The products recalled are the following lot numbers: 300010, 300011, 300012, 300013, 300014, 300015, 300016, 300017 and 300018. These lots were manufactured between Feb. 3, 2016, and Jan. 14, 2018 and distributed between the dates of March 18, 2016, and Jan. 17, 2018.
FDA Recall of the MindFrameCapture LP Revascularization Device was issued May 18, 2018. In February 2018, medical providers were told to remove these devices from inventory and quarantine them, and then return them to the manufacturer, Medtronic.