Medtronic Catheter Recall Lawsuit
The Sutureless Connector intrathecal catheter and the IsoMed constant-flow fusion pump, when combined, has now been classified as a Class 1 recall by the FDA. The recall was issued after a statement was issued by Medtronic Inc. warning of the risks posed by the catheter and the infusion pump when the two are used together.
Because the Infusion pump and the catheter only pose a risk when they are combined they are still able to be produced. The products are also only considered Class 1 recalled when they are combined since they pose no risk when used separately. The recall is about the SC Catheter and Revision Kit models 8709SC, 8731SC, 8578SC, and 8596SC when combined with model 8472 IsoMed Pump. The IsoMed Pump model 8472 was discontinued in September of 2008.