Medtronic Pacemaker Lawsuit Medtronic Pacemaker
 
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Medtronic Pain Pumps Recalled

-InjuryBoard.com

09/30/2008- The FDA has issued a recall for Medtronic drug pumps. The recall notice came Friday. The pumps involved are the Indura 1P Intrathecal Catheter, model 8709SC; Intrathecal Catheter, model 8731SC; Sutureless Pump Connector Revision Kit, model 8578, and Intrathecal Catheter Pump Segment Revision Kit, model 8596SC. The pumps are used in patients who have spasticity related to cystic fibrosis, traumatic brain injury and multiple sclerosis and from chronic pain.

The FDA issued a Class I recall which means that there is a "reasonable probability" that the product may cause serious adverse health consequences or death. Improper connections between the implanted catheter and the pump cause the medications to leak. At least 25,000 of these pumps have been sold.

If you or a loved one have had the device replaced or plan to have it replaced you may be entitled to compensation regardless if you suffered as a result of complications from surgery or the device itself. Contact the Medtronic attorneys of Ennis & Ennis today for a free confidential case evaluation. Our on staff nurse and lawyers are standing by to answer any questions you may have regarding the Medtronic pacemaker defects, a possible Medtronic class action lawsuit, or any other type of Medtronic Pacemaker litigation.

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