Inside pamphlet there is a section that I did not pay much attention to which says that if you have a central line and mistakenly insert any of this product, it can cause blood fungal infection. I do not have a central line - I have a port-a-cath which is implanted and is permanent. It is only accessed once a month. The contraindication goes on to say that this warning also applies to all ports. I called the company and they basically re-read the insert to me and said I should see a doctor for questions. I was alarmed but will discontinue the product. I was hopeful about its potential before this. Anything else I should do?