| My son contacted Pseudomonos Aeruginosa during a failed cord blood bone marrow transplant in Feb. after using a Clinipad dressing change kit this year. Have been trying to retrieve information from the FDA on the Clinipad Corp. and Pseudomonos Aeruginosa with no luck. Much info on the web about the facility that manf. the dressing change kit being shutdown for the same bacteria found in their sterile products. My question is being a parent do I have any rights to the information that I know they have from all the press releases on the web without the use of the legal system? Have not been able to secure an attorney yet but have only discussed it with one. He did survive septic shock and 17 days life support in PICU and a total of 28 days in the hospital from this bacteria. Also would like to know if the home health company that supplied all the supplies to us should carry any of the fault since we were not notified even after his 28 day hospital stay. We still have approx. 500 pcs of recalled Clinipad products in our supplies whitch we have stopped using. If we would not have changed home health companies we would have still been using this product. Also what responsiblility does the doctor hold in reporting this infection to the FDA? | 
Linear Mode
