Ennis & Ennis, P.A. is representing individuals that have been harmed as a result of Medtronic defibrillator or pacemaker defects. If you or a loved one have been injured you may be entitled to compensation. For more information about your legal rights or for more information regarding the Medtronic recall click here to contact one of our Medtronic Attorneys about a Medtronic lawsuit today.
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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.
Ennis & Ennis, P.A. is representing individuals that have been harmed by defective medical devices such as the Medtronic defibrillator and pacemaker. If you or a loved one have suffered as a result of a defective Medtronic pacemaker or defibrillator or if you need more information about the Medtronic recall or class action lawsuit click here for a free, confidential case evaluation.
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