News of the recall initiated by Cordis Corporation in regards to several lots of its line of balloon catheters used in angioplasty procedures has led to an urgent need for several things, including immediate medical attention for those who depend on these products, legal help for those who have suffered injuries as a result of using them and information regarding potential side effects so that patients can gain an understanding of what to watch for in regards to their own health.
Below is a brief description of the side effects associated with this FDA-announced recall, and if you are experiencing any of these symptoms, seek medical help immediately and then contact a defective medical products attorney to schedule an initial consultation.
Foundational Description of Balloon CathetersBalloon catheters are supposed to be used during an angioplasty procedure to unblock the artery or blood vessels around the heart that are filled with plaque that creates the medical issue in the first place. Once inside, these catheters are supposed to deflate and allow the vessel or artery to continue operating without the substance that’s been blocking it.
^ Back To TopThere are three potential side effects that have been identified with these defective medical products. They are as follows:
Of course, one ‘side effect’ that is not listed can be the result
of any or all of the conditions described above – death to the patient
as a result of heart failure. If you or someone you love is depending
on the Cordis products that have been recalled, you need to seek medical attention
immediately. If your diagnosis is such that you’ve been injured
as a result of these products, contact a defective products attorney as soon
as possible to schedule an initial consultation.
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